Home NDC 78691-037 BIOPURE Hand Sanitizer Spray-Coastal Glow
Product NDC 78691-037
11-digit product format 786910037
Labeler code 78691
Product ID 78691-037_4876717b-45ca-60ce-e063-6394a90af2b1
Type HUMAN OTC DRUG
Nonproprietary name Hand Sanitizer Spray
Dosage form LIQUID
Route TOPICAL
Labeler Quest USA Corp
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-15
Substance ALCOHOL
Active strength 16 g/30mL
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 BIOPURE Hand Sanitizer Spray-Coastal Glow
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 16 g/30mL
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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 78691-037-00 BIOPURE Hand Sanitizer Spray-Coastal Glow 30 mL in 1 BOTTLE, SPRAY LIQUID 30 2
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 44 of 114 · 2,277 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 78691-037-00 78691003700 30 mL in 1 BOTTLE, SPRAY (78691-037-00) 30 ml 2026-01-15 No No Current