"49967-099-01" National Drug Code (NDC)

NDC Code	49967-099-01
Package Description	50 mL in 1 JAR (49967-099-01)
Product NDC	49967-099
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Kiehls Since 1851 Ultra Facial Broad Spectrum Spf 30 Sunscreen
Non-Proprietary Name	Avobenzone, Homosalate, Octisalate And Octocrylene
Dosage Form	CREAM
Usage	TOPICAL
Start Marketing Date	20151101
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M020
Manufacturer	L�Oreal USA Products Inc
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength	30; 50; 50; 70
Strength Unit	mg/mL; mg/mL; mg/mL; mg/mL