"37808-726-10" National Drug Code (NDC)

NDC Code	37808-726-10
Package Description	28.3 g in 1 PACKAGE (37808-726-10)
Product NDC	37808-726
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Sunscreen
Non-Proprietary Name	Octinoxate, Octisalate, Zinc Oxide
Dosage Form	GEL
Usage	TOPICAL
Start Marketing Date	20170606
Marketing Category Name	OTC MONOGRAPH FINAL
Application Number	part352
Manufacturer	HEB
Substance Name	OCTINOXATE; OCTISALATE; ZINC OXIDE
Strength	562; 250; 1000
Strength Unit	g/g; g/g; g/g
Pharmacy Classes	Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]