Home NDC 87302-214-14 VANILLA SCENT HAND SANITIZER
Product NDC 87302-214
Requested package NDC 87302-214-14
11-digit product format 873020214
Labeler code 87302
Product ID 87302-214_c454f2f5-245e-4108-ace2-02e88755eac9
Type HUMAN OTC DRUG
Nonproprietary name ETHYL ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler Amber Glow Cosmetics Limited
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-05
Substance ALCOHOL
Active strength 70 mL/100mL
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base VANILLA SCENT HAND SANITIZER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581662 Internal RxNorm 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 Status 87302-214-14 87302021414 30 mL in 1 BOTTLE, PLASTIC (87302-214-14) 30 ml 2026-06-05 0 Current