AIBRAVE
AIBRAVE is an FDA drug label for the active ingredient GYNECOLOGICAL INTIMATE CARE GEL manufactured by Tupelo Brittany LLC 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 20260823.
- Generic name
- GYNECOLOGICAL INTIMATE CARE GEL
- Manufacturer
- Tupelo Brittany LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87854-002
- Application
- 505G(a)(3)
- Label effective
- 20260823
About this product
AIBRAVE is an FDA-registered drug product whose active ingredient is GYNECOLOGICAL INTIMATE CARE GEL. It is labelled by Tupelo Brittany LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87854-002, application 505G(a)(3), label effective 20260823. It is one of 2 FDA drug label records sharing the active ingredient GYNECOLOGICAL INTIMATE CARE GEL. 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 GYNECOLOGICAL INTIMATE CARE GEL are most often described in connection with: hands open, intimate area, discard applicator, one application. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Directions After washing your hands, open the packremove the cap, and apply it to the intimate area. Discard applicator after one application.
Dosage & Administration
When using this product 1. After opening the cap, use the product immediately and do not reuse it 2. avoid contact with eyes; if contact occurs, rinse thoroughly with water 3. mild temporary tingling may occur 4. do not share applicators
Warnings
Warnings For external and intravaginal use only When using this product 1. After opening the cap, use the product immediately and do not reuse it 2. avoid contact with eyes; if contact occurs, rinse thoroughly with water 3. mild temporary tingling may occur 4. do not share applicators
More products with the same ingredient
GYNECOLOGICAL INTIMATE CARE GELHow products containing GYNECOLOGICAL INTIMATE CARE GEL compare
FDA lists 2 drug label records with GYNECOLOGICAL INTIMATE CARE GEL 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 |
|---|---|---|---|
| — | — | Tupelo Brittany LLC | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is AIBRAVE used for?
Directions After washing your hands, open the packremove the cap, and apply it to the intimate area. Discard applicator after one application.
Who makes AIBRAVE?
Tupelo Brittany LLC is the labeler of record for AIBRAVE. 2 FDA label records share the active ingredient GYNECOLOGICAL INTIMATE CARE GEL, 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 AIBRAVE 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 AIBRAVE 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 GYNECOLOGICAL INTIMATE CARE GEL?
Yes. 2 FDA drug label records list GYNECOLOGICAL INTIMATE CARE GEL 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 AIBRAVE 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.