Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride

Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride is an FDA-registered drug product whose active ingredient is PRAMOXINE HYDROCHLORIDE. It is labelled by The Honey Pot Company LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82637-9363, application M017, label effective 20260610. It is one of 8 FDA drug label records sharing the active ingredient PRAMOXINE HYDROCHLORIDE. 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 PRAMOXINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, itching associated, minor skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves pain and itching associated with minor skin irritations

Directions: Adults and children 12 years of age and children under 12 years of age • Consult a doctor • Apply to affected area not more than 3 or 4 times daily. Children under 12 years of age: Consult a doctor

Warnings: For external use only When using this product: avoid contact with eyes. Stop use and ask doctor if: Condition worsens If symptoms persist for more than 7 days, or clear up and reoccur again withing a few days Keep out of reach of of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

FDA lists 8 drug label records with PRAMOXINE HYDROCHLORIDE 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 Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride used for?
Uses temporarily relieves pain and itching associated with minor skin irritations

Who makes Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride?
The Honey Pot Company LLC is the labeler of record for Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride. 8 FDA label records share the active ingredient PRAMOXINE HYDROCHLORIDE, 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 Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride 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 Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride 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 PRAMOXINE HYDROCHLORIDE?
Yes. 8 FDA drug label records list PRAMOXINE HYDROCHLORIDE 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 Anti-Itch Soothing Wipes 1 Pramoxine Hydrochloride 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.