"51239-2921-0" National Drug Code (NDC)

NDC Code	51239-2921-0
Package Description	7 g in 1 POUCH (51239-2921-0)
Product NDC	51239-2921
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Scrubs Sunscreen
Non-Proprietary Name	Sunscreen
Dosage Form	LOTION
Usage	TOPICAL
Start Marketing Date	20170501
End Marketing Date	20241201
Marketing Category Name	OTC MONOGRAPH FINAL
Application Number	part352
Manufacturer	ITW Pro Brands
Substance Name	AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength	.01; .05; .075; .05; .06
Strength Unit	g/g; g/g; g/g; g/g; g/g