"37808-914-12" National Drug Code (NDC)

NDC Code	37808-914-12
Package Description	237 mL in 1 TUBE (37808-914-12)
Product NDC	37808-914
Product Type Name	HUMAN OTC DRUG
Proprietary Name	H.e.b Ultra
Non-Proprietary Name	Spf 50 Sunscreen
Dosage Form	AEROSOL, SPRAY
Usage	TOPICAL
Start Marketing Date	20190205
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M020
Manufacturer	H.E.B
Substance Name	AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength	30; 100; 45; 80
Strength Unit	mg/mL; mg/mL; mg/mL; mg/mL