Scalpicin Anti-Itch Maximum Strength

Scalpicin Anti-Itch Maximum Strength is an FDA-registered drug product whose active ingredient is HYDROCORTISONE. It is labelled by Reckitt Benckiser LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 63824-851, application M017, label effective 20260513. 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: temporarily relieves, itching associated, minor skin, rashes due, seborrheic dermatitis, eczema psoriasis, supervision doctor. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves itching associated with minor skin irritations and rashes due to seborrheic dermatitis eczema psoriasis other uses of this product should be only under the advice and supervision of a doctor

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 twist the flow-control cap to open apply at first signs of itching if using after shampooing, towel dry hair apply from bottle directly to scalp, massage in to avoid running or dripping, do not squeeze bottle too hard

Warnings For external use only Avoid contact with the eyes If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, stop use of this product and do not begin use of any other hydrocortisone product unless you have consulted a doctor Do not use for the treatment of diaper rash. Consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Scalpicin Anti-Itch Maximum Strength used for?
Uses temporarily relieves itching associated with minor skin irritations and rashes due to seborrheic dermatitis eczema psoriasis other uses of this product should be only under the advice and supervision of a doctor

Who makes Scalpicin Anti-Itch Maximum Strength?
Reckitt Benckiser LLC is the labeler of record for Scalpicin Anti-Itch Maximum Strength. 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 Scalpicin Anti-Itch Maximum Strength 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 Scalpicin Anti-Itch Maximum Strength 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 Scalpicin Anti-Itch Maximum Strength been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.