0.9% Benzyl Alcohol Solution (Laboratory Use Only)

Product NDC: 87710-002
Requested package NDC: 87710-002-01
11-digit product format: 877100002
Labeler code: 87710
Product ID: 87710-002_5976bde6-099a-ffc4-e063-6394a90aadcf
Type: HUMAN OTC DRUG
Nonproprietary name: 0.9% Benzyl Alcohol Solution (Laboratory Use Only)
Dosage form: LIQUID
Route: CUTANEOUS
Labeler: Guangzhou Huanmei Cosmetics Co., Ltd
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2026-08-20
Substance: BENZYL ALCOHOL
Active strength: .9 mg/100mg
Pharmacologic classes: Pediculicide [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: 0.9% Benzyl Alcohol Solution (Laboratory Use Only)
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZYL ALCOHOL	.9 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
LKG8494WBH	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5976bde6-0999-ffc4-e063-6394a90aadcf	Available on FDA.report

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0.9% Benzyl Alcohol Solution (Laboratory Use Only)	0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY)	Guangzhou Huanmei Cosmetics Co., Ltd	5976bde6-0999-ffc4-e063-6394a90aadcf	2026-08-20	Warnings	Exact identifier ndc (package): 87710-002-01 ndc (product): 87710-002 ndc11 (package): 87710000201

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LKG8494WBH	BENZYL ALCOHOL	100-51-6	BENZYL ALCOHOL

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
87710-002-01	87710000201	1 BOTTLE in 1 BOX (87710-002-01) / 30 mg in 1 BOTTLE	1 bottle	2026-08-20	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
0.9% Benzyl Alcohol Solution (Laboratory Use Only)	Guangzhou Huanmei Cosmetics Co., Ltd \| Guangzhou Huanmei Cosmetics Co., Ltd.	2026-08-20	HUMAN OTC DRUG LABEL	1