SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION

SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION is an FDA-registered drug product whose active ingredient is ALUMINUM CHLORIDE. It is labelled by DC Alpine Partners, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 54913-011, application M019, label effective 20260623. It is one of 8 FDA drug label records sharing the active ingredient ALUMINUM CHLORIDE. 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 ALUMINUM CHLORIDE are most often described in connection with: apply apply, bedtime gently, press clean, dry skin, rub air, morning wash, treated area. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

HOW TO APPLY: 1. Apply at night, before bedtime. 2. Gently press to clean, dry skin (do not rub). 3. Air dry for 5 minutes and go to bed. 4. In the morning, wash the treated area.

Directions Apply at bedtime. Ensure skin is clean and dry. Use every 7 days, or as needed.

Warnings For external use only. Do not use on broken or irritated skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center immediately.

FDA lists 8 drug label records with ALUMINUM CHLORIDE 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 SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION used for?
HOW TO APPLY: 1. Apply at night, before bedtime. 2. Gently press to clean, dry skin (do not rub). 3. Air dry for 5 minutes and go to bed. 4. In the morning, wash the treated area.

Who makes SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION?
DC Alpine Partners, LLC is the labeler of record for SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION. 8 FDA label records share the active ingredient ALUMINUM CHLORIDE, 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 SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION 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 SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION 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 ALUMINUM CHLORIDE?
Yes. 8 FDA drug label records list ALUMINUM CHLORIDE 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 SWEATBLOCK ORIGINAL MAXIMUM CLINICAL PROTECTION 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.