Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla
Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla is an FDA drug label for the active ingredient ANTIPERSPIRANT DEODORANT manufactured by Suave Brands Company 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 20260522.
- Generic name
- ANTIPERSPIRANT DEODORANT
- Manufacturer
- Suave Brands Company
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83711-138
- Application
- M019
- Label effective
- 20260522
About this product
Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla is an FDA-registered drug product whose active ingredient is ANTIPERSPIRANT DEODORANT. It is labelled by Suave Brands Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83711-138, application M019, label effective 20260522. It is one of 2 FDA drug label records sharing the active ingredient ANTIPERSPIRANT DEODORANT. 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 ANTIPERSPIRANT DEODORANT 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
Use reduces underarm wetness
Dosage & Administration
Directions apply to underarms only
Warnings
Warnings For external use only Do not use on broken skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
More products with the same ingredient
ANTIPERSPIRANT DEODORANTHow products containing ANTIPERSPIRANT DEODORANT compare
FDA lists 2 drug label records with ANTIPERSPIRANT DEODORANT 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 |
|---|---|---|---|
| — | — | Guangzhou Charm Beauty Trading Co., Ltd. | 1 |
| — | — | Suave Brands Company | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla used for?
Use reduces underarm wetness
Who makes Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla?
Suave Brands Company is the labeler of record for Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla. 2 FDA label records share the active ingredient ANTIPERSPIRANT DEODORANT, 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 Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla 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 Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla 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 ANTIPERSPIRANT DEODORANT?
Yes. 2 FDA drug label records list ANTIPERSPIRANT DEODORANT 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 Suave Invisible Solid Antiperspirant Deodorant Lavender and Vanilla 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.