COCONUT ANTIBACTERIAL HAND SANITIZER
COCONUT ANTIBACTERIAL HAND SANITIZER is an FDA drug label for the active ingredient ALCOHOL manufactured by ENCHANTE ACCESSORIES 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 20260627.
- Generic name
- ALCOHOL
- Manufacturer
- ENCHANTE ACCESSORIES INC.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 50563-476
- Application
- M003
- Label effective
- 20260627
About this product
COCONUT ANTIBACTERIAL HAND SANITIZER is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by ENCHANTE ACCESSORIES INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 50563-476, application M003, label effective 20260627. It is one of 582 FDA drug label records sharing the active ingredient ALCOHOL. 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 ALCOHOL are most often described in connection with: decrease bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Dosage & Administration
Directions Wet hands thoroughly with product and allow to dry without wiping. For Children under 6, use under adult supervision Not recommended for infants.
Warnings
Warnings For external use only-hands. Flammable. Keep away from heat and flame. When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if Skin irritation develops. Use under adult supervision. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center Immediately.
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View labelHow products containing ALCOHOL compare
FDA lists 582 drug label records with ALCOHOL 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 |
|---|---|---|---|
| — | — | Bath & Body Works, Inc. | 79 |
| — | — | Shenzhen Lantern Scicence Co.,Ltd. | 66 |
| — | — | Fourstar Group USA, Inc. | 41 |
| — | — | Church & Dwight Co., Inc. | 33 |
| — | — | Target Corporation | 23 |
Frequently asked questions
What is COCONUT ANTIBACTERIAL HAND SANITIZER used for?
Use To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Who makes COCONUT ANTIBACTERIAL HAND SANITIZER?
ENCHANTE ACCESSORIES INC. is the labeler of record for COCONUT ANTIBACTERIAL HAND SANITIZER. 582 FDA label records share the active ingredient ALCOHOL, 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 COCONUT ANTIBACTERIAL HAND SANITIZER 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 COCONUT ANTIBACTERIAL HAND SANITIZER 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 ALCOHOL?
Yes. 582 FDA drug label records list ALCOHOL 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 COCONUT ANTIBACTERIAL HAND SANITIZER 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.