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Hydrocortisone Plus 12 Moisturizers Maximum Strength

Dosage form: cream
Ingredients: HYDROCORTISONE 1g in 100g
Labeler: L&R Distributors, Inc.
NDC Code: 15127-919

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Hydrocortisone Cream Maximum Strength Plus 12 - Select Brand

 Drug Facts


Active ingredient

Hydrocortisone, USP 1%

Purpose

Anti-itch

Uses 

for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to:

eczema   insect bites   • poison ivy   • poison oak   • poison sumac   • soaps

• jewelry   • detergents    • cosmetics   • psoriasis        • seborrheic dermatitis

• for external genital, feminine and anal itching    • other uses of this product should be only under the advice and supervision of a doctor

Warnings

For external use only

Do not use

for external feminine itching if you have a vaginal discharge. Consult a doctor.
• for the treatment of diaper rash. Consult a doctor.

When using this product

• avoid contact with the eyes   • do not begin the use of any other hydrocortisone product unless directed by a doctor   • for external anal itching:  • do not use more than directed unless directed by a doctor   • do not put this product into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

• symptoms last for more than 7 days   • the condition gets worse   • symptoms clear up and occur again in a few days   • rectal bleeding occurs, consult doctor promptly

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older
• apply to affected area not more than 3 to 4 times daily
Children under 2 years of age
• do not use, consult a doctor
For external anal itching
Adults: when practical, clean the affected area with mild soap and warm water, rinse thoroughly, gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product
Children under 12 years of age: consult a doctor

Other information

• Store at room temperature 59°-86 °F (15°-30°C). Protect from freezing.
• Before using any medication, read all label directions. Keep carton, it contains important information.

Inactive ingredients

aloe concentrate, cetostearyl alcohol, cetyl alcohol, corn oil, glycerin, glyceryl stearate, isopropyl myristate, isopropyl palmitate, methylparaben, mineral oil, polyoxyl 40 stearate, polysorbate 60, propylene glycol, propylparaben, purified water, sorbic acid, sorbitan monostearate, stearyl alcohol, vitamin A, vitamin D, vitamin E, white petrolatum, white wax. May contain citric acid or sodium citrate solution to adjust pH.

Questions? 

1-800-432-8534 between 9 am and 4 pm EST, Monday-Friday.

PRINCIPAL DISPLAY PANEL

select brand®
the lower price name brand 

NDC 15127-919-01 

MAXIMUM STRENGTH
Anti-Itch Cream
Hydrocortisone Cream, USP 1%
Plus 12 Moisturizers With Aloe
Itch and Rash Relief
Compare to the active ingredient of Cortizone•10® Plus Maximum Strength

NET WT 1 OZ (28g)

HYDROCORTISONE  PLUS 12 MOISTURIZERS MAXIMUM STRENGTH
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-919
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (HYDROCORTISONE) HYDROCORTISONE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE 
CETOSTEARYL ALCOHOL 
CETYL ALCOHOL 
CITRIC ACID MONOHYDRATE 
CORN OIL 
GLYCERIN 
GLYCERYL MONOSTEARATE 
ISOPROPYL MYRISTATE 
ISOPROPYL PALMITATE 
METHYLPARABEN 
MINERAL OIL 
POLYOXYL 40 STEARATE 
POLYSORBATE 60 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SODIUM CITRATE 
SORBIC ACID 
SORBITAN MONOSTEARATE 
STEARYL ALCOHOL 
VITAMIN A 
VITAMIN D 
ALPHA-TOCOPHEROL 
PETROLATUM 
WHITE WAX 
Packaging
#Item CodePackage Description
1NDC:15127-919-011 TUBE in 1 CARTON
128 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34804/05/2010
Labeler - L&R Distributors, Inc. (012578514)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

 
L&R Distributors, Inc.

Medically reviewed on Nov 13, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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