Biopure

Product NDC
78691-029
11-digit product format
786910029
Labeler code
78691
Product ID
78691-029_324b205c-dbba-7a6b-e063-6394a90ab184
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
2025-04-15
Substance
ALCOHOL
Active strength
16 g/30mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Biopure
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL16 g/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3K9958V90M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78691-029-01Biopure30 mL in 1 BOTTLE, SPRAYLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78691-029BIOPURE (HAND SANITIZER SPRAY) LIQUID [QUEST USA CORP]1Current NDC, 1 package rows20250416_324b140d-9d43-1c2f-e063-6294a90ae303.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
78691-029-017869100290130 mL in 1 BOTTLE, SPRAY (78691-029-01) 30 ml2025-04-15NoNoHistorical