"76229-123-01" National Drug Code (NDC)

NDC Code	76229-123-01
Package Description	1 BOTTLE in 1 PACKAGE (76229-123-01) / 85 mL in 1 BOTTLE
Product NDC	76229-123
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Likewise Hand Moisturizer - Sun Protectant Spf 50
Non-Proprietary Name	Octinoxate, Octisalate, Zinc Oxide
Dosage Form	CREAM
Usage	TOPICAL
Start Marketing Date	20110620
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M020
Manufacturer	Likewise Incorporated
Substance Name	OCTINOXATE; OCTISALATE; ZINC OXIDE
Strength	75; 50; 111.6
Strength Unit	mg/mL; mg/mL; mg/mL