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(EYE oh dyne)

Index Terms

  • Iodoflex
  • Iodosorb

Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tincture, External:

GoodSense Iodine: (30 mL)

Generic: 2% (30 mL, 473 mL, 500 mL, 4000 mL, 20000 mL); 7% (59 mL, 480 mL)

Brand Names: U.S.

  • GoodSense Iodine [OTC]

Pharmacologic Category

  • Antiseptic, Topical


Iodine is required for thyroid hormone synthesis. Iodine is also known to be a powerful broad spectrum germicidal agent effective against a wide range of bacteria, viruses, fungi, protozoa, and spores. Iodosorb® and Iodoflex™ contain iodine in hydrophilic beads of cadexomer which allows a slow release of iodine into the wound and absorption of fluid, bacteria, and other substances from the wound


Topical: Amount absorbed systemically depends upon concentration and characteristics of skin


Primarily trapped by the thyroid


Degraded by amylases normally present in wound fluid


Urine (>90%)

Use: Labeled Indications

Used topically as an antiseptic in the management of minor, superficial skin wounds and has been used to disinfect the skin preoperatively


Hypersensitivity to iodine or any component of the formulation

Iodosorb, Iodoflex: Hashimoto thyroiditis, history of Grave’s disease, or nontoxic nodular goiter; pregnancy; breastfeeding

Dosing: Adult

Cleaning wet ulcers and wounds (Iodosorb, Iodoflex): Topical: Apply to clean wound; maximum: 50 g/application and 150 g/week. Change dressing ~3 times/week; reduce applications as exudate decreases. Do not use for >3 months; discontinue when wound is free of exudate.

Antiseptic for minor cuts, scrapes, burns: Topical: Apply small amount to affected area 1 to 3 times/day

Dosing: Geriatric

Refer to adult dosing.

Dosing: Pediatric

Antiseptic for minor cuts, scrapes, burns: Children and Adolescents: Topical: Apply small amount to affected area 1 to 3 times daily


Topical: Iodosorb®: Apply 1/8" to 1/4" thickness to dry sterile gauze, then place prepared gauze onto clean wound. Change dressing when gel changes color from brown to yellow/gray (~3 times/week). Remove with sterile water, saline, or wound cleanser; gently blot fluid from surface leaving wound slightly moist before reapplying gel.


Store at room temperature.

Drug Interactions

Sodium Iodide I131: Iodine may diminish the therapeutic effect of Sodium Iodide I131. Management: Discontinue topical iodine at least 3 weeks before sodium iodide I-131 administration, and avoid concurrent use. Avoid combination

Test Interactions

Large amounts from excessive absorption may alter thyroid function tests.

Adverse Reactions

The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.

Topical: Frequency not defined.

Dermatologic: Eczema, localized erythema

Endocrine & metabolic: Increased thyroid stimulating hormone level

Hypersensitivity: Hypersensitivity reaction

Local: Local irritation, local pain, localized edema

Reactions reported more likely observed following large doses or chronic iodine intoxication; frequency not defined.

Central nervous system: Headache, metallic taste

Dermatologic: Acne vulgaris, skin rash (including ioderma), urticaria

Endocrine & metabolic: Hypothyroidism

Gastrointestinal: Diarrhea

Hematologic & oncologic: Adenopathy, eosinophilia, mucous membrane bleeding

Hypersensitivity: Angioedema

Neuromuscular & skeletal: Arthralgia

Ophthalmic: Eyelid edema

Respiratory: Pulmonary edema

Miscellaneous: Fever


Disease-related concerns:

• Renal impairment: Use with caution in patients with renal impairment.

Dosage form specific issues:

• Iodosorb: For use as topical application to wet wounds only.

Other warnings/precautions:

• Appropriate use: Not for application to large areas of the body or for use with tight or air-excluding bandages. When used as a topical antiseptic, improper use may lead to product contamination. Although infrequent, product contamination has been associated with reports of localized and systemic infections. To reduce the risk of infection, ensure antiseptic products are used according to the labeled instructions; avoid diluting products after opening; and apply single-use containers only one time to one patient and discard any unused solution (FDA Drug Safety Communication, 2013).

• OTC labeling: When used for self-medication (OTC), do not use on deep wounds, puncture wounds, animal bites, or serious burns without consulting with health care provider. Notify healthcare provider if condition does not improve within 7 days.

Monitoring Parameters

Thyroid function should be monitored in pregnant women, neonates, and young infants if repeat applications over large areas are needed.

Pregnancy Considerations

An adequate amount of iodine intake is essential for thyroid function. Iodine crosses the placenta and requirements are increased during pregnancy. Iodine deficiency in pregnancy can lead to neurologic damage in the newborn; an extreme form, cretinism, is characterized by gross mental retardation, short stature, deaf mutism, and spasticity. Large amounts of iodine during pregnancy can cause fetal goiter or hyperthyroidism. Transient hypothyroidism in the newborn has also been reported following topical or vaginal use prior to delivery.

Further information

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