Ingredients:

Manufacturer
Guangzhou Huanmei Cosmetics Co., Ltd | Guangzhou Huanmei Cosmetics Co., Ltd.
Effective date
2026-08-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-26 01:01:38

Label at a glance#

Product0.9% Benzyl Alcohol Solution (Laboratory Use Only)
Active ingredientBENZYL ALCOHOL
Label structure9 sections

Indications and uses

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 hig...

Dosage and administration

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.

Label contents#

Full prescribing information#

Ingredients:

INACTIVE INGREDIENT SECTION

Deionized Water, 0.9% BenzyI Alcohol

Intended use

OTC - PURPOSE SECTION

For Research Only

OTHER SAFETY

OTHER SAFETY INFORMATION

Antiseptic:
Inhibit bacteria & mould to keep solution sterile;
Solubilizer:
to avoid stratification;
Dissolve peptides & lipophilic active ingredients
Penetration aid:
In vitro penetration research test;
Irritation buffer:materials.
Reduce irritation of high-concentration raw

Notice:

WARNINGS SECTION

Keep sealed afteruse.Discard if turbid.
Not for injection, skin application or oral intake.
Store in cool & dark place, keep away from kids.

Directions for Use:

DOSAGE & ADMINISTRATION SECTION

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.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION


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.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of children. Store in a cool, dark place.

Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

non

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL

0202

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87710-00287710-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0.9% Benzyl Alcohol Solution (Laboratory Use Only)0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY)Guangzhou Huanmei Cosmetics Co., Ltd5976bde6-0999-ffc4-e063-6394a90aadcf2026-08-20WarningsExact identifier
ndc (package): 87710-002-01
ndc (product): 87710-002
ndc11 (package): 87710000201
spl id: 5976bde6-099a-ffc4-e063-6394a90aadcf
spl set id: 5976bde6-0999-ffc4-e063-6394a90aadcf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.