Babyganics - 51514-0235-1 - (Octinoxate, Octisalate, and Zinc)

Alphabetical Index


Drug Information of Babyganics

Product NDC: 51514-0235
Proprietary Name: Babyganics
Non Proprietary Name: Octinoxate, Octisalate, and Zinc
Active Ingredient(s): 7.5; 5; 11.2    mL/100mL; mL/100mL; mL/100mL & nbsp;   Octinoxate, Octisalate, and Zinc
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Babyganics

Product NDC: 51514-0235
Labeler Name: Autumn Harp, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120223

Package Information of Babyganics

Package NDC: 51514-0235-1
Package Description: 177 mL in 1 BOTTLE (51514-0235-1)

NDC Information of Babyganics

NDC Code 51514-0235-1
Proprietary Name Babyganics
Package Description 177 mL in 1 BOTTLE (51514-0235-1)
Product NDC 51514-0235
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate, and Zinc
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20120223
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Autumn Harp, Inc.
Substance Name OCTINOXATE; OCTISALATE; ZINC OXIDE
Strength Number 7.5; 5; 11.2
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Babyganics


General Information