Home NDC 87710-002 0.9% Benzyl Alcohol Solution (Laboratory Use Only)
Product NDC 87710-002
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.
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.
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