Anti itch
Anti itch is an FDA drug label for the active ingredient HYDROCORTISONE manufactured by Weeks & Leo Co., Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231212.
Generic: HYDROCORTISONE
Manufacturer: Weeks & Leo Co., Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 11383-292
Application: M017
Effective: 20231212
Active Ingredients: Active Ingredient Hydrocortisone 1 %
Indications & Usage
Uses for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to: eczema seborrheic dermatitis psoriasis insect bites poison ivy, poison oak, and poison sumac cosmetics jewelry detergents soaps temporarily relieves external anal and genital itching other uses of this product should be only under the advice and supervision of a doctor
Dosage & Administration
Directions adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily children under 2 years: ask a doctor
Contraindications
Not available.
Warnings
Warnings For external use only When using this product do not get into the eyes Do not use for the treatment of diaper rash. Ask a doctor. Stop us and ask doctor if condition gets worse, or if symptoms last for more than 7 days or clear up and occur again within a few days. Do not begin use of any other hydrocortisone product. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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