Carpe Antiperspirant Sandalwood
Carpe Antiperspirant Sandalwood is an FDA drug label for the active ingredient ALUMINUM. SESQUICHLOROHYDRATE 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. SESQUICHLOROHYDRATE
- Manufacturer
- Clutch Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 74307-821
- Application
- M019
- Label effective
- 20260820
About this product
Carpe Antiperspirant Sandalwood is an FDA-registered drug product whose active ingredient is ALUMINUM. SESQUICHLOROHYDRATE. It is labelled by Clutch Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 74307-821, application M019, label effective 20260820. It is one of 16 FDA drug label records sharing the active ingredient ALUMINUM. SESQUICHLOROHYDRATE. 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. SESQUICHLOROHYDRATE 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
Reduces underarm perspiration.
Dosage & Administration
Apply to underarms only Rotate knob to dispense product and rub in vigorously Apply every night before going to bed and again in the morning
Warnings
For external use only. Do not use on broken or irritated skin Stop use and ask a doctor if rash or irritation occurs Ask a doctor before use if you have kidney disease
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ALUMINUM. SESQUICHLOROHYDRATECarpe Antiperspirant Amber Dusk
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View labelHow products containing ALUMINUM. SESQUICHLOROHYDRATE compare
FDA lists 16 drug label records with ALUMINUM. SESQUICHLOROHYDRATE 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 |
|---|---|---|---|
| — | — | Clutch Inc | 16 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Carpe Antiperspirant Sandalwood used for?
Reduces underarm perspiration.
Who makes Carpe Antiperspirant Sandalwood?
Clutch Inc is the labeler of record for Carpe Antiperspirant Sandalwood. 16 FDA label records share the active ingredient ALUMINUM. SESQUICHLOROHYDRATE, 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 Carpe Antiperspirant Sandalwood 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 Carpe Antiperspirant Sandalwood 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. SESQUICHLOROHYDRATE?
Yes. 16 FDA drug label records list ALUMINUM. SESQUICHLOROHYDRATE 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 Carpe Antiperspirant Sandalwood 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.