Medi-First Hydrocortisone 1 % Anti-Itch Cream

Medi-First Hydrocortisone 1 % Anti-Itch Cream is an FDA-registered drug product whose active ingredient is HYDROCORTISONE. It is labelled by Unifirst First Aid Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 47682-866, application M017, label effective 20260616. It is one of 81 FDA drug label records sharing the active ingredient HYDROCORTISONE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing HYDROCORTISONE are most often described in connection with: temporary relief, itching associated, minor skin, irritations inflammation, rashes due, eczema psoriasis, poison ivy, sumac insect. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Uses for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to: eczema psoriasis poison ivy poison oak poison sumac insect bites detergents jewlery seborrheic dermatitis soaps for external genital, feminine and anal itching other uses of this product should bew under the advice and supervision of a doctor

Directions Directions For itiching of skin irritation, inflamation, and rashes adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily for children under 2 years of age: do not use, consult a doctor For external anal and genitial itching adults and children 12 years and older when practical, cleanse the ffected area with mild soap and warm water and rinse throroughly gently dry by patting or blotting with toilet tissue or a soft cloth before applying apply to affected area not more than 3 to 4 times daily children under 12 years if age: consult a doctor

Warnings Warnings For external use only.

FDA lists 81 drug label records with HYDROCORTISONE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Medi-First Hydrocortisone 1 % Anti-Itch Cream used for?
Uses Uses for the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to: eczema psoriasis poison ivy poison oak poison sumac insect bites detergents jewlery seborrheic dermatitis soaps for external genital, feminine and anal itching other uses of this product should bew under the advice and supervision of a doctor

Who makes Medi-First Hydrocortisone 1 % Anti-Itch Cream?
Unifirst First Aid Corporation is the labeler of record for Medi-First Hydrocortisone 1 % Anti-Itch Cream. 81 FDA label records share the active ingredient HYDROCORTISONE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Medi-First Hydrocortisone 1 % Anti-Itch Cream come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Medi-First Hydrocortisone 1 % Anti-Itch Cream prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing HYDROCORTISONE?
Yes. 81 FDA drug label records list HYDROCORTISONE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Medi-First Hydrocortisone 1 % Anti-Itch Cream been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.