2OZ BRAZZILLIAN AP DEODORANT ASST
2OZ BRAZZILLIAN AP DEODORANT ASST is an FDA drug label for the active ingredient ALUMINUM CHLOROHYDRATE manufactured by Rejoice International Corp. 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 20260421.
- Generic name
- ALUMINUM CHLOROHYDRATE
- Manufacturer
- Rejoice International Corp.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 57337-191
- Application
- M019
- Label effective
- 20260421
About this product
2OZ BRAZZILLIAN AP DEODORANT ASST is an FDA-registered drug product whose active ingredient is ALUMINUM CHLOROHYDRATE. It is labelled by Rejoice International Corp. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 57337-191, application M019, label effective 20260421. It is one of 20 FDA drug label records sharing the active ingredient ALUMINUM CHLOROHYDRATE. 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 CHLOROHYDRATE are most often described in connection with: reduces underarm. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Reduces underarm wetness and perspiration.
Dosage & Administration
Directions Remove cap. Turn dial to raise product. Apply evenly to underarms only. Replace cap after use.
Warnings
Warnings For external use only. Do not use Do not use on broken skin Ask a doctor before use if Ask a doctor before use if you have kidney disease. Stop use and ask a doctor if Stop use and ask a doctor if irritation or rash develops. Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.
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View labelHow products containing ALUMINUM CHLOROHYDRATE compare
FDA lists 20 drug label records with ALUMINUM CHLOROHYDRATE 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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | The Procter & Gamble Manufacturing Company | 4 |
| — | — | Zhongke Pharmaceutical (Foshan) Co., Ltd. | 4 |
| — | — | L'Oreal USA Products Inc | 2 |
| — | — | CLINIQUE LABORATORIES LLC | 1 |
| — | — | China Ningbo Shangge Cosmetics Technology Corp. | 1 |
Frequently asked questions
What is 2OZ BRAZZILLIAN AP DEODORANT ASST used for?
Uses Reduces underarm wetness and perspiration.
Who makes 2OZ BRAZZILLIAN AP DEODORANT ASST?
Rejoice International Corp. is the labeler of record for 2OZ BRAZZILLIAN AP DEODORANT ASST. 20 FDA label records share the active ingredient ALUMINUM CHLOROHYDRATE, 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 2OZ BRAZZILLIAN AP DEODORANT ASST 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 2OZ BRAZZILLIAN AP DEODORANT ASST 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 CHLOROHYDRATE?
Yes. 20 FDA drug label records list ALUMINUM CHLOROHYDRATE 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 2OZ BRAZZILLIAN AP DEODORANT ASST 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.