"49967-907-03" National Drug Code (NDC)

NDC Code	49967-907-03
Package Description	1 TUBE in 1 CARTON (49967-907-03) / 5 mL in 1 TUBE
Product NDC	49967-907
Product Type Name	HUMAN OTC DRUG
Proprietary Name	La Roche Posay Laboratoire Dermatologique
Proprietary Name Suffix	Anthelios 50 Mineral Ultra Light Sunscreen
Non-Proprietary Name	Titanium Dioxide And Zinc Oxide
Dosage Form	LOTION
Usage	TOPICAL
Start Marketing Date	20110701
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M020
Manufacturer	L'Oreal USA Products Inc
Substance Name	TITANIUM DIOXIDE; ZINC OXIDE
Strength	60; 50
Strength Unit	mg/mL; mg/mL