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ATOMY SUNSCREEN
ATOMY SUNSCREEN - 52257-1230-1 - (Octinoxate, Octisalate, Zinc Oxide, Titanium Dioxide)
Drug Information of ATOMY SUNSCREEN
| Product NDC: | 52257-1230 |
| Proprietary Name: | ATOMY SUNSCREEN |
| 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) |
Labeler Information of ATOMY SUNSCREEN
| Product NDC: | 52257-1230 |
| 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 Information of ATOMY SUNSCREEN
| Package NDC: | 52257-1230-1 |
| Package Description: | 60 mL in 1 CARTON (52257-1230-1) |
NDC Information of ATOMY SUNSCREEN
| NDC Code | 52257-1230-1 |
| Proprietary Name | ATOMY SUNSCREEN |
| Package Description | 60 mL in 1 CARTON (52257-1230-1) |
| Product NDC | 52257-1230 |
| 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 |
