0.9% Benzyl Alcohol Solution (Laboratory Use Only)
0.9% Benzyl Alcohol Solution (Laboratory Use Only) is an FDA drug label for the active ingredient 0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY) manufactured by Guangzhou Huanmei Cosmetics Co., Ltd administered by CUTANEOUS. 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
- 0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY)
- Manufacturer
- Guangzhou Huanmei Cosmetics Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- CUTANEOUS
- Dosage form
- N/A
- NDC
- 87710-002
- Application
- N/A
- Label effective
- 20260820
About this product
0.9% Benzyl Alcohol Solution (Laboratory Use Only) is an FDA-registered drug product whose active ingredient is 0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY). It is labelled by Guangzhou Huanmei Cosmetics Co., Ltd taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 87710-002, label effective 20260820. 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 0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY) are most often described in connection with: usage bacteriostatic, benzyl alcohol, research applications, solution inhibit, mould growth, solubilizer dissolve, lipophilic active, help prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
INDICATIONS AND USAGE Bacteriostatic Water with 0.9% Benzyl Alcohol is intended for research use only. It may be used in research applications as a bacteriostatic solution to inhibit bacterial and mould growth, as a solubilizer to dissolve peptides and lipophilic active ingredients and help prevent stratification, as a penetration aid for in vitro penetration testing, and as an irritation buffer to reduce irritation associated with high-concentration raw materials. This product is not intended for injection, skin application, or oral intake.
Dosage & Administration
Directions for Use: For research use only. Use as required according to the applicable research protocol. The product may be used as a bacteriostatic aqueous solution, solubilizer, penetration aid, or irritation buffer for in vitro research applications. Keep the container sealed after use. Not for injection, skin application, or oral intake.
Warnings
Notice: Keep sealed afteruse.Discard if turbid. Not for injection, skin application or oral intake. Store in cool & dark place, keep away from kids.
Frequently asked questions
What is 0.9% Benzyl Alcohol Solution (Laboratory Use Only) used for?
INDICATIONS AND USAGE Bacteriostatic Water with 0.9% Benzyl Alcohol is intended for research use only. It may be used in research applications as a bacteriostatic solution to inhibit bacterial and mould growth, as a solubilizer to dissolve peptides and lipophilic active ingredients and help prevent stratification, as a penetration aid for in vitro penetration testing, and as an irritation buffer …
Who makes 0.9% Benzyl Alcohol Solution (Laboratory Use Only)?
Guangzhou Huanmei Cosmetics Co., Ltd is the labeler of record for 0.9% Benzyl Alcohol Solution (Laboratory Use Only).
What form does 0.9% Benzyl Alcohol Solution (Laboratory Use Only) come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is 0.9% Benzyl Alcohol Solution (Laboratory Use Only) 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.
Has 0.9% Benzyl Alcohol Solution (Laboratory Use Only) 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.