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