Dosage and administration
Apply to affected area 3 to 4 times daily in accordance with physician's directions.
Hydrocortisone 1% - lodoquinol 1% Cream
- Manufacturer
- Westminster Pharmaceuticals, LLC
- Effective date
- 2020-09-24
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:50:07
Label at a glance#
ProductHydrocortisone Iodoquinol
Active ingredientHYDROCORTISONE, IODOQUINOL
Label structure13 sections
Storage and handling
Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (between 59°F to 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized. Keep container tightly closed. Protect from freezing and excessive heat.
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Rx Only
DESCRIPTION
Each gram contains 10 mg of hydrocortisone and 10 mg of iodoquinol in a vehicle consisting of: cetyl alcohol, glycerin, glyceryl stearate SE, mineral oil, PEG-100 stearate, phenoxyethanol, purified water, stearyl alcohol, white petrolatum, xanthan gum.
Paraben Free.
Chemically, hydrocortisone is [Pregn-4-ene-3, 20-dione, 11, 17, 21-trihydroxy-, (11β)-] with the molecular formula C21H30O5) and is represented by the following structural formula:
and iodoquinol, 5, 7-diiodo-8-quinolinol (C9H5I2NO) is represented by the following structural formula:
Hydrocortisone is an anti-inflammatory and antipruritic agent, while iodoquinol is an antifungal and antibacterial agent.
CLINICAL PHARMACOLOGY
Hydrocortisone has an anti-inflammatory, antipruritic and vasoconstrictive properties. While the mechanism of anti-inflammatory activity is unclear, there is evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and the therapeutic efficacy in humans lodoquinol has both antifungal and antibacterial properties.
Pharmacokinetics
The extent of the percutaneous absorption of topical steroids is determined by many factors including the vehicle, the integrity of the epidermal barrier and the use of occlusive dressings. Hydrocortisone can be absorbed from normal intact skin. Inflammation and/or other inflammatory disease processes in the skin increase percutaneous absorption. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. Once absorbed through the skin, hydrocortisone is metabolized in the liver and most body tissue to hydrogeneted and degraded forms such as tetrahydrocortisone and tetrahydrocortisol. These are excreted in the urine, mainly conjugated as glucuronides, together with a very small proportion of unchanged hydrocortisone. There are no data available regarding the percutaneous absorption of iodoquinol; however, following oral administration, 3-5% of the dose was recovered in the urine as glucuronide.
INDICATIONS
Based on a review of a related drug by the National Research Council and subsequent FDA classification for that drug, the indications are as follows: "Possibly" Effective: Contact or atopic dermatitis; impetiginized eczema; nummular eczema; endogenous chronic infectious dermatitis; stasis dermatitis; pyoderma; nuchal eczema and chronic eczematoid otitis externa; acne urticata; localized or disseminated neurodermatitis; lichen simplex chronicus; anogenital pruritus (vulvae, scroti, ani); folliculitis; bacterial dermatoses; mycotic dermatoses such as tinea (capitis, cruris, corporis, pedis); moniliasis; intertrigo. Final classification of the less-than-effective indications requires further investigation.
CONTRAINDICATIONS
This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.
WARNING
FOR EXTERNAL USE ONLY.
PRECAUTIONS
NOT FOR OPHTHALMIC USE.
KEEP OUT OF REACH OF CHILDREN.
Avoid contact with eyes, lips and mucous membranes.
Information for Patients
If irritation develops, the use of this product should be discontinued and appropriate therapy instituted. Staining of the skin, hair and fabrics may occur. Not intended for the use on infants or under diapers of occlusive dressings. If extensive areas are treated or if the occlusive dressing technique is used, the possibility exists of increased systemic absorption of the corticosteroid, and suitable precautions should be taken.
Children may absorb proportionally larger amounts of topical corticosteroids and thus be more susceptible to systemic toxicity.
Iodoquinol may be absorbed through the skin and interfere with thyroid function tests. If such tests are contemplated, wait at least one month after discontinuance of therapy to perform these tests. The ferric chloride test for phenylketonuria (PKU) can yield a false positive result if iodoquinol is present in the diaper or urine. Prolonged use may result on overgrowth of non-susceptible organisms requiring appropriate therapy.
Carcinogenesis, Mutagenesis and Impairment of Fertility
Long-term animal studies for carcinogenic potential have not been performed on this product to date. In vitro studies to determine mutagenicity with hydrocortisone have revealed negative results. Mutagenicity studies have not been performed with iodoquinol.
Pregnancy
Category C
Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.
Nursing Mothers
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this product is administered to a nursing woman.
Pediatric Use
Safety and effectiveness in pediatric patients under the age of 12 have not been established.
ADVERSE REACTIONS
The following local adverse reactions are reported infrequently with topical corticosteroids. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infections, skin atrophy, striae and miliaria.
DOSAGE AND ADMINISTRATION
Apply to affected area 3 to 4 times daily in accordance with physician's directions.
STORAGE
Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (between 59°F to 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized. Keep container tightly closed.
NOTICE
Protect from freezing and excessive heat.
HOW SUPPLIED
1 oz. tubes, NDC 69367-286-01
To report a serious adverse event or obtain product information, call 1-844-221-7294.
SPL UNCLASSIFIED SECTION
Manufactured for:
Westminster Pharmaceuticals, LLC
Nashville, TN 37217
Rev. 01/23
PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton
NDC 69367-286-01
Rx Only
Hydrocortisone 1%-Iodoquinol 1% Cream
Westminster
Pharmaceuticals
Net Wt 1 oz (28.4 g)
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69367-286-01 | GM - Gram | 69367-286 | 3b242e0a-f863-4458-97e3-51755446f523 | 1 | 2021-01-08 |
Products#
Every source-derived product name is available through these pages.
- Hydrocortisone Iodoquinol
- Hydrocortisone and Iodoquinol
- HYDROCORTISONE
- IODOQUINOL
- CETYL ALCOHOL
- GLYCERYL STEARATE SE
- MINERAL OIL
- WATER
- STEARYL ALCOHOL
- XANTHAN GUM
- GLYCERIN
- PEG-100 STEARATE
- PHENOXYETHANOL
- WHITE PETROLATUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69367-286 | 69367-286-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| IODOQUINOL | 63W7IE88K8 | ACTIB |
| CETYL ALCOHOL | 936JST6JCN | IACT |
| GLYCERYL STEARATE SE | FCZ5MH785I | IACT |
| MINERAL OIL | T5L8T28FGP | IACT |
| WATER | 059QF0KO0R | IACT |
| STEARYL ALCOHOL | 2KR89I4H1Y | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PEG-100 STEARATE | YD01N1999R | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| WHITE PETROLATUM | B6E5W8RQJ4 | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 394fb503-308a-457d-9ab9-3e32d7e5ec66 | e468f033-4bf8-4786-92be-09d230065d9c | 2020-09-24 | Warnings, Adverse reactions | 394fb503-308a-457d-9ab9-3e32d7e5ec66 e468f033-4bf8-4786-92be-09d230065d9c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.