Class: Anti-inflammatory Agents
ATC Class: D07AB10
VA Class: DE200
Chemical Name: (7α,11β,16α)-7-Chloro-11-hydroxy-16-methyl-17,21-bis (1-oxopropoxy)pregna-1,4-diene-3,20-dione
Molecular Formula: C28H37ClO7
CAS Number: 66734-13-2
A synthetic corticosteroid.1 2 12 d
Uses for Alclometasone Dipropionate
Relief of inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.1 4 5 6 7 8 9 10 11 13 14 17 18 d
Generally most effective in acute or chronic dermatoses (e.g., seborrheic or atopic dermatitis, localized neurodermatitis, anogenital pruritus, psoriasis, late phase of allergic contact dermatitis, inflammatory phase of xerosis).b
Topical therapy generally preferred over systemic therapy; fewer associated adverse systemic effects.b
Topical therapy generally only controls manifestations of dermatoses; eliminate cause if possible.b
Topical efficacy may be increased by using a higher concentration or occlusive dressing therapy. (See Administration with Occlusive Dressing under Dosage and Administration.)b
Response may vary from one topical corticosteroid preparation to another.b
Anti-inflammatory activity may vary considerably depending on the vehicle, drug concentration, site of application, disease, and individual patient.b
Manufacturers state that alclometasone should not be used for the treatment of acne, rosacea, or perioral dermatitis.22 23
Alclometasone dipropionate 0.05% cream and ointment are considered to have low-to-medium range potency.b c d
Alclometasone Dipropionate Dosage and Administration
Consider location of the lesion and the condition being treated when choosing a dosage form.b
Creams are suitable for most dermatoses, but ointments may also provide some occlusion and are usually used for the treatment of dry, scaly lesions.b
Formulation affects percutaneous penetration and subsequent activity; extemporaneous preparation or dilution of commercially available products with another vehicle may decrease effectiveness.b
Patients applying a topical corticosteroid to a large surface area and/or to areas under occlusion should be evaluated periodically for evidence of hypothalamic-pituitary-adrenal (HPA)-axis suppression by appropriate endocrine testing (e.g., ACTH stimulation, plasma cortisol, urinary free cortisol).c d (See Hypothalamic-Pituitary-Adrenal Axis Suppression and also Systemic Effects, under Cautions.)
For dermatologic use only; avoid contact with eyes.d
Apply creams and ointments topically to the skin or scalp.c
The area of skin to be treated may be thoroughly cleansed before topical application to reduce the risk of infection; however, some clinicians believe that, unless an occlusive dressing is used, cleansing of the treated area is unnecessary and may be irritating.b
Apply cream or ointment sparingly in a thin film and rub gently into the affected area.1 d
After a favorable response is achieved, frequency of application or concentration (strength) may be decreased to the minimum necessary to maintain control and to avoid relapse; discontinue if possible.b
Administration with Occlusive Dressing
Occlusive dressings may be used for severe or resistant dermatoses (e.g., psoriasis).1 17 (See Occlusive Dressings under Cautions.)
Soak or wash the affected area to remove scales; apply a thin film of cream or ointment; rub gently into the lesion; and apply another thin film.b Cover affected area with a thin, pliable plastic film and seal it to adjacent normal skin with adhesive tape or hold in place with a gauze or elastic bandage.b
If affected area is moist, incompletely seal the edges of the plastic film or puncture the film to allow excess moisture to escape.b For added moisture in dry lesions, apply cream or ointment and cover with a dampened cloth before the plastic film is applied or briefly soak the affected area in water before application of the drug and plastic film.b
Thin polyethylene gloves may be used on the hands and fingers, plastic garment bags may be used on the trunk or buttocks, a tight shower cap may be used for the scalp, or whole-body suits may be used instead of plastic film to provide occlusion.b
Frequency of occlusive dressing changes depends on the condition being treated; cleansing of the skin and reapplication of the corticosteroid are essential at each dressing change.b
Occlusive dressing is usually left in place for 12–24 hours and therapy is repeated as needed.b Although occlusive dressing may be left in place for 3–4 days at a time in resistant conditions, most clinicians recommend intermittent use of occlusive dressings for 12 hours daily to reduce the risk of adverse effects (particularly infection) and systemic absorption and for greater convenience.b
The drug and an occlusive dressing may be used at night, and the drug or a bland emollient may be used without an occlusive dressing during the day.b
In patients with extensive lesions, sequential occlusion of only one portion of the body at a time may be preferable to whole-body occlusion.b (See Occlusive Dressings under Cautions.)
Administer the least amount of topical preparations that provide effective therapy.b (See Pediatric Use under Cautions.)
Children ≥1 year of age: Apply cream or ointment sparingly 2–3 times daily.1 d
Discontinue when control is achieved; if improvement does not occur within 2 weeks, consider reassessment of the diagnosis.c d
Apply cream or ointment sparingly 2–3 times daily.1 d
May be used for 2–6 weeks5 6 7 8 9 10 11 13 14 18 ; however, more prolonged therapy23 with appropriate monitoring17 may be necessary in patients with resistant or chronic conditions.a
Discontinue when control is achieved; if improvement does not occur within 2 weeks, consider reassessment of the diagnosis.c d
Children ≥1 year of age: Maximum 3 weeks.c
No specific dosage recommendations at this time.c d
No specific dosage recommendations at this time.c d
Careful dosage selection recommended.d
Cautions for Alclometasone Dipropionate
Known hypersensitivity to alclometasone, other corticosteroids, or any ingredient in the formulation.1 d
Allergic contact dermatitis may manifest as failure to heal rather than irritation as occurs with other topical preparations that do not contain corticosteroids; confirm with diagnostic patch testing.b c d
Hypothalamic-Pituitary-Adrenal Axis Suppression
Topically applied corticosteroids can be absorbed in sufficient amounts to reversibly suppress the HPA axis.c d
Perform periodic HPA-axis evaluation by appropriate testing (e.g., ACTH stimulation, morning plasma cortisol, urinary free cortisol), especially in patients applying a topical corticosteroid to a large surface area or to areas under occlusion.b c d
If HPA-axis suppression occurs, withdraw the drug, reduce the frequency of application, and/or substitute a less potent corticosteroid.c d
HPA-axis function recovery generally is prompt and complete following drug discontinuance.c d
Rarely, glucocorticosteroid insufficiency may require systemic corticosteroid therapy.b c d
Systemic absorption following topical administration may result in manifestations of Cushing’s syndrome, hyperglycemia, and glucosuria in some patients.b c d
Adverse systemic effects may occur when corticosteroids are used on large areas of the body, for prolonged periods of time, with an occlusive dressing, and/or concurrently with other corticosteroid-containing preparations.b
Infants and children may be more susceptible to adverse systemic effects.c d (See Pediatric Use under Cautions.)
Possible adverse local reactions (e.g., burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, miliaria); may occur more frequently with the use of occlusive dressings, especially with prolonged therapy.b
Prolonged use of topical corticosteroids may cause atrophy of the epidermis and subcutaneous tissue;b these effects are most likely to occur (even with short-term use) in intertriginous (e.g., axilla, groin), flexor, and facial areas.b
If irritation occurs, discontinue drug and institute appropriate therapy.c d
If concurrent skin infection is present or develops, initiate appropriate anti-infective therapy.c d If infection does not respond promptly, discontinue topical corticosteroid therapy until the infection has been controlled.c d
When topical corticosteroids and topical anti-infectives are used concomitantly, consider that the corticosteroid may mask clinical signs of bacterial, fungal, or viral infections; prevent recognition of ineffectiveness of the anti-infective; or suppress hypersensitivity reactions to ingredients in the formulation.b In addition, consider the cautions, precautions, and contraindications associated with the anti-infective.b (See Occlusive Dressings under Cautions.)
Some manufacturers state that topical corticosteroids are contraindicated in patients with tuberculosis of the skin, dermatologic fungal infections, and cutaneous or systemic viral infection (including vaccinia and varicella and herpes simplex of the eye or adjacent skin).b However, most clinicians believe topical corticosteroids can be used with caution if the infection is treated.b
Adverse systemic corticosteroid effects may occur with use of occlusive dressings on large areas of the body and for prolonged periods of time; monitor accordingly.b (See Hypothalamic-Pituitary-Adrenal Axis Suppression and also see Systemic Effects, under Cautions.)
Adverse local reactions may occur more frequently with the use of occlusive dressings, especially with prolonged therapy.b c d (See Local Effects under Cautions.)
Do not use occlusive dressings on weeping or exudative lesions.b
Do not use occlusive dressings in patients with primary skin infection.b
Remove occlusive dressings covering large areas if body temperature increases; thermal homeostasis may be impaired.b
Use plastic occlusive material with care to avoid the risk of suffocation.b
Category C.c d
Not known whether topical alclometasone is distributed into milk.c d Caution advised if topical alclometasone is used.c d
Safety and efficacy not established in children <1 year of age.c d
Do not use for the treatment of diaper dermatitis; tight-fitting diapers or plastic pants should not be used on a child being treated with alclometasone in the diaper area, since such garments may constitute occlusive dressings.c d
Children are more susceptible to topical corticosteroid-induced HPA-axis suppression and Cushing’s syndrome than mature individuals because of a greater skin surface area-to-body weight ratio, especially when topical corticosteroids are applied to >20% of body surface area.c d The risk of adrenal suppression appears to increase with decreasing age.b (See Systemic Effects under Cautions.)
Manifestations of adrenal suppression in children include linear growth retardation, delayed weight gain, low plasma cortisol concentrations, and lack of response to corticotropin (ACTH) stimulation.b c d
Children also are at greater risk of glucocorticoid insufficiency during and/or after withdrawal of treatment.b c d
Intracranial hypertension has occurred in children; manifestations include bulging fontanelles, headaches, and bilateral papilledema.b c d
Striae have been reported in children treated inappropriately with topical corticosteroids.b c d
Topical corticosteroid therapy in children should be limited to the minimum amount necessary for therapeutic efficacy; chronic topical corticosteroid therapy may interfere with growth and development.b
Response in limited number of patients ≥65 years of age does not appear to differ from that in younger adults.c d
Common Adverse Effects
Burning, itching, erythema, irritation,, dryness, papular rash, folliculitis, acneiform eruptions, hypopigmentationc , perioral dermatitis, allergic contact dermatitis, secondary infection, skin atrophy, striae, miliaria.c d
Interactions for Alclometasone Dipropionate
Specific Drugs and Laboratory Tests
Drug or Test
Nitroblue-tetrazolium test for bacterial infection
Concurrent use of corticosteroids reportedly may result in false-negative resultsb
Alclometasone Dipropionate Pharmacokinetics
Topically applied alclometasone can be absorbed through normal intact skin.4 22 b c d
Percutaneous penetration varies among individuals14 and can be altered by using occlusive dressings,1 4 16 17 d high corticosteroid concentrations, and certain vehicles.1 15 16 b d
Only minimal amounts of topical corticosteroid reach the dermis and subsequently the systemic circulation after application to most normal skin areas; more absorption occurs from the scrotum, axilla, eyelid, face, and scalp than from the forearm, knee, elbow, palm, and sole.b
Absorption is markedly increased by loss of the skin’s keratin layer and by inflammation and/or diseases of the epidermal barrier (e.g., psoriasis, eczema).1 16 17 b d
Not known whether topical alclometasone is distributed into milk.c d
Once absorbed through the skin, topically applied corticosteroids are metabolized primarily in the liver.22 b
Topical corticosteroids and metabolites are excreted by the kidneys and, to a lesser extent, in bile.1 22
Cream and ointment: 2–30°C.1 Some manufacturers state 20–25°C.d Consult product information for specific recommendations.
Precise mechanism of action for topical anti-inflammatory activity is unknown; therapeutic benefit in the management of corticosteroid-responsive dermatoses mediated primarily through anti-inflammatory, antipruritic, and vasoconstrictive actions.c d
Anti-inflammatory effects may occur through induction of phospholipase A2 inhibitory proteins (lipocortins); decreased arachidonic acid release from membrane phospholipids.d Decreased arachidonic acid precursors may downregulate biosynthesis of potent inflammatory mediators (e.g., prostaglandins, leukotrienes).d
Decreases inflammation by stabilizing leukocyte lysosomal membranes, preventing release of destructive acid hydrolases from leukocytes; inhibiting macrophage accumulation in inflamed areas; reducing leukocyte adhesion to capillary endothelium; reducing capillary wall permeability and edema formation; decreasing complement components; antagonizing histamine activity and release of kinin from substrates; reducing fibroblast proliferation, collagen deposition, and subsequent scar tissue formation; and possibly by other mechanisms as yet unknown.b
Advice to Patients
Importance of using only as directed, only for the disorder for which it was prescribed, and for no longer than prescribed; avoid contact with the eyes and only apply externally as directed.c d (See Topical Administration under Dosage and Administration.)
Importance of not applying on the face, underarms, or groin unless directed by clinician.c d
Importance of informing patients that treated areas of the skin should not be bandaged or otherwise covered or wrapped as to be occlusive unless directed by a clinician.c d
Importance of reporting any local adverse reactions, especially those occurring under occlusive bandage, to a clinician.b c d
Importance of informing parents of children not to use in the treatment of diaper dermatitis and not to apply in the diaper area as diapers or plastic pants may constitute occlusive dressings.c d
Importance of discontinuing use when control is achieved; importance of contacting clinician if no improvement is seen in 2 weeks.c d
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.c d
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.c d
Importance of advising patients of other important precautionary information. (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Alclometasone Dipropionate Cream (with propylene glycol)
Aclovate (with propylene glycol)
Alclometasone Dipropionate Ointment
Aclovate (with propylene glycol)
AHFS DI Essentials. © Copyright 2017, Selected Revisions January 1, 2008. American Society of Health-System Pharmacists, Inc., 4500 East-West Highway, Suite 900, Bethesda, Maryland 20814.
1. Glaxo Inc. Aclovate prescribing information. Research Triangle Park, NC; 1986 Sep.
2. Windholz M, ed. The Merck index. 10th ed. Rahway, NJ: Merck & Co, Inc; 1983:34.
3. Cornell RC, Stoughton RB. Correlation of the vasoconstriction assay and clinical activity in psoriasis. Arch Dermatol. 1985; 121:63-7. [PubMed 3881088]
4. Thornfeldt C, Cornell RC, Stoughton RB. The effect of alclometasone dipropionate cream 0.05% on the hypothalamic-pituitary-adrenal axis of normal volunteers. J Int Med Res. 1985; 13:276-80. [PubMed 4054428]
5. Lassus A. Clinical comparison of alclometasone dipropionate cream 0.05% with hydrocortisone butyrate cream 0.1% in the treatment of atopic dermatitis in children. J Int Med Res. 1983; 11:315-9. [PubMed 6357892]
6. Bagatell FK, Barkoff JR, Cohen HJ et al. A multicenter comparison of alclometasone dipropionate cream 0.05% and hydrocortisone cream 1.0% in the treatment of atopic dermatitis. Curr Ther Res. 1983; 33:46-52.
7. Cornell RC. Atrophogenic potential of alclometasone dipropionate ointment 0.05% vs hydrocortisone ointment 1.0%. Curr Ther Res. 1986; 39:260-8.
8. Kalivas J, Kanof NB, Miller OF III et al. A controlled clinical comparison of alclometasone dipropionate cream 0.05% and hydrocortisone cream 1.0% in patients with psoriasis. Curr Ther Res. 1983; 33:408-14.
9. Aggerwal A, Maddin S. Alclometasone dipropionate in psoriasis: a clinical study. J Int Med Res. 1982; 10:414-8. [PubMed 7152079]
10. Frost P. Clinical comparison of alclometasone dipropionate and desonide ointments (0.05%) in the management of psoriasis. J Int Med Res. 1982; 10:375-8. [PubMed 6754511]
11. Lassus A. Alclometasone dipropionate cream 0.05% versus clobetasone butyrate cream 0.05%: a controlled clinical comparison in the treatment of atopic dermatitis in children. Int J Dermatol. 1984; 23:565-6. [PubMed 6389385]
12. Green MJ, Berkenkopf J, Xiomara F et al. Synthesis and structure-activity relationships in a novel series of topically active corticosteroids. J Steroid Biochem. 1979; 11:61-6. [PubMed 491605]
13. Duke EE, Maddin S, Aggerwal A. Alclometasone dipropionate in atopic dermatitis: a clinical study. Curr Ther Res. 1983; 33:769-74.
14. Crespi HG. Topical corticosteroid therapy for children: alclometasone dipropionate cream 0.05%. Clin Ther. 1986; 8:203-10. [PubMed 2938740]
15. Cornell RC, Stoughton RB. The use of topical steroids in psoriasis. Dermatol Clin. 1984; 2:397-409.
16. Cornell RC, Stoughton RB. Use of glucocorticosteroids in psoriasis. Pharmacol Ther. 1980; 2:497-508.
17. Food and Drug Administration. Topical corticosteroids class labeling guideline. (Undated.) Available from: Professional Labeling Branch, Division of Drug Advertising and Labeling, Food and Drug Administration, Rockville, MD.
18. Mobacken H, Hersle K. Alclometasone dipropionate ointment 0.05% versus hydrocortisone ointment 1.0% in children with eczema. Acta Ther. 1986; 12:269-78.
19. Green MJ, Shue HJ, Tiberi R et al. The influence of esterification on the topical antiinflammatory activity of 7 alpha-chloro- and 7 alpha-bromo-16 alpha-methylprednisolones. Arzneimittelforschung. 1980; 30:1618-20. [PubMed 7192095]
20. Lutsky BN, Berkenkopf J, Fernandez X et al. Selective effects of 7 alpha-halogeno substitution on corticosteroid activity: Sch 22219 and Sch 23409. Arzneimittelforschung. 1979; 29:992-8. [PubMed 583002]
21. Lutsky BN, Berkenkopf J, Fernandez X et al. A novel class of potent topical antiinflammatory agents: 17-benzoylated, 7 alpha-halogeno substituted corticosteroids. Arzneimittelforschung. 1979; 29:1662-7. [PubMed 543873]
22. Vonderweidt J (Glaxo, Research Triangle Park, NC): Personal communication; 1987 Apr 15.
23. Reviewers’ comments (personal observations); 1987 Apr.
24. Tokiwa T, Oyama T, Kimura S et al. [Studies on the primary dermal irritation, ocular mucosa irritation and local anaesthetic effect of alclometasone dipropionate (ADP)]. (Japanese; with English abstract.) Oyo Yakuri. 1986; 32:937-43.
25. Fujii K, Uda F, Yamamoto K. [Phototoxicity and photosensitivity tests of alclometasone dipropionate (ADP).] (Japanese; with English abstract.) Oyo Yakuri. 1986; 32:945-51.
26. Hasegawa T, Tujita K, Fujino A et al. [Immunogenicity study on alclometasone dipropionate (ADP)]. (Japanese; with English abstract.) Oyo Yakuri. 1986; 32:953-60.
27. Sills J (Schering, Kenilworth, NJ): Personal communication; 1987 May 28.
28. Lechner D (Schering, Kenilworth, NJ): Personal communication; 1987 June 3.
a. AHFS drug information 2007. McEvoy GK, ed. Alclometasone dipropionate. Bethesda, MD: American Society of Health-Systems Pharmacists; 2007: 3525–6.
b. AHFS drug information 2007 McEvoy GK, ed. Topical corticosteroids general statement. Bethesda, MD: American Society of Health-System Pharmacists; 2007:3423–5.
c. GlaxoSmithKline. Aclovate (alclometasone dipropionate) cream and ointment 0.05% prescribing information. Pittsburgh, PA; 2002 Aug.
d. Taro Pharmaceuticals. Alclometasone dipropionate ointment USP, 0.05% prescribing information. Hawthorne, NY; 2004 Jul.
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