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ATOMY SUN CREAM SPF 50 PA
ATOMY SUN CREAM SPF 50 PA - 52257-1001-2 - (OCTINOXATE)
Drug Information of ATOMY SUN CREAM SPF 50 PA
| Product NDC: | 52257-1001 |
| Proprietary Name: | ATOMY SUN CREAM SPF 50 PA |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 4.5; 3; 1.5; 2.9 mL/60mL; mL/60mL; mL/60mL; mL/60mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ATOMY SUN CREAM SPF 50 PA
| Product NDC: | 52257-1001 |
| Labeler Name: | ATOMY CO LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100428 |
Package Information of ATOMY SUN CREAM SPF 50 PA
| Package NDC: | 52257-1001-2 |
| Package Description: | 1 TUBE in 1 BOX (52257-1001-2) > 60 mL in 1 TUBE (52257-1001-1) |
NDC Information of ATOMY SUN CREAM SPF 50 PA
| NDC Code | 52257-1001-2 |
| Proprietary Name | ATOMY SUN CREAM SPF 50 PA |
| Package Description | 1 TUBE in 1 BOX (52257-1001-2) > 60 mL in 1 TUBE (52257-1001-1) |
| Product NDC | 52257-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100428 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ATOMY CO LTD |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 4.5; 3; 1.5; 2.9 |
| Strength Unit | mL/60mL; mL/60mL; mL/60mL; mL/60mL |
| Pharmaceutical Classes |
