Hand Antiperspirant Nightly Use
Hand Antiperspirant Nightly Use is an FDA drug label for the active ingredient ALUMINUM CHLORIDE HEXAHYDRATE manufactured by Clutch 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 20260820.
- Generic name
- ALUMINUM CHLORIDE HEXAHYDRATE
- Manufacturer
- Clutch Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 74307-008
- Application
- M019
- Label effective
- 20260820
About this product
Hand Antiperspirant Nightly Use is an FDA-registered drug product whose active ingredient is ALUMINUM CHLORIDE HEXAHYDRATE. It is labelled by Clutch Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 74307-008, application M019, label effective 20260820. 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.
What it is used for
Across FDA labelling, products containing ALUMINUM CHLORIDE HEXAHYDRATE are most often described in connection with: ask doctor, rash irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Stop use and ask a doctor if rash or irritation occurs
Dosage & Administration
Directions Wash and dry hands thoroughly before application Apply a single pump of product to palms each morning Rub palms together vigorously for 30 seconds
Warnings
Warnings For external use only. Do not use on broken or irritated skin Ask a doctor before use if you have kidney disease.
Frequently asked questions
What is Hand Antiperspirant Nightly Use used for?
Stop use and ask a doctor if rash or irritation occurs
Who makes Hand Antiperspirant Nightly Use?
Clutch Inc is the labeler of record for Hand Antiperspirant Nightly Use.
What form does Hand Antiperspirant Nightly Use 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 Hand Antiperspirant Nightly Use 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.
Has Hand Antiperspirant Nightly Use 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.