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Coppertone Sensitive Skin
Coppertone Sensitive Skin - 11523-7300-2 - (Octinoxate, Octisalate, and Zinc Oxide)
Drug Information of Coppertone Sensitive Skin
| Product NDC: | 11523-7300 |
| Proprietary Name: | Coppertone Sensitive Skin |
| Non Proprietary Name: | Octinoxate, Octisalate, and Zinc Oxide |
| Active Ingredient(s): | 85.2; 56.8; 164.72 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate, and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Coppertone Sensitive Skin
| Product NDC: | 11523-7300 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990521 |
Package Information of Coppertone Sensitive Skin
| Package NDC: | 11523-7300-2 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (11523-7300-2) |
NDC Information of Coppertone Sensitive Skin
| NDC Code | 11523-7300-2 |
| Proprietary Name | Coppertone Sensitive Skin |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (11523-7300-2) |
| Product NDC | 11523-7300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19990521 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 85.2; 56.8; 164.72 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
