Sanell Hand Sanitizer
Drug Facts
Approved
Approval ID
7184b9ad-0125-413d-b054-f46239b8ca92
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 28, 2025
Manufacturers
FDA
OraLabs
DUNS: 801824756
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Alcohol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63645-177
Application NumberM003
Product Classification
M
Marketing Category
C200263
G
Generic Name
Alcohol
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 28, 2025
FDA Product Classification
INGREDIENTS (2)
WATERInactive
Quantity: 2.6857 mL in 7.5 mL
Code: 059QF0KO0R
Classification: IACT
ALCOHOLActive
Quantity: 4.275 mL in 7.5 mL
Code: 3K9958V90M
Classification: ACTIB