Product NDC: | 52257-1220 |
Proprietary Name: | Atomy Sunscreen White |
Non Proprietary Name: | Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide |
Active Ingredient(s): | 4.08; 2.7; 2.92; 8.06 mg/60mL; mg/60mL; mg/60mL; mg/60mL & nbsp; Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52257-1220 |
Labeler Name: | ATOMY CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130201 |
Package NDC: | 52257-1220-1 |
Package Description: | 60 mL in 1 CARTON (52257-1220-1) |
NDC Code | 52257-1220-1 |
Proprietary Name | Atomy Sunscreen White |
Package Description | 60 mL in 1 CARTON (52257-1220-1) |
Product NDC | 52257-1220 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ATOMY CO., LTD. |
Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 4.08; 2.7; 2.92; 8.06 |
Strength Unit | mg/60mL; mg/60mL; mg/60mL; mg/60mL |
Pharmaceutical Classes |