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Coppertone Dry
Coppertone Dry - 11523-7340-1 - (Homosalate, Octinoxate, Octisalate, and Oxybenzone)
Drug Information of Coppertone Dry
| Product NDC: | 11523-7340 |
| Proprietary Name: | Coppertone Dry |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 42.2; 63.3; 42.2; 25.32 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Coppertone Dry
| Product NDC: | 11523-7340 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120201 |
Package Information of Coppertone Dry
| Package NDC: | 11523-7340-1 |
| Package Description: | 177 mL in 1 BOTTLE, PUMP (11523-7340-1) |
NDC Information of Coppertone Dry
| NDC Code | 11523-7340-1 |
| Proprietary Name | Coppertone Dry |
| Package Description | 177 mL in 1 BOTTLE, PUMP (11523-7340-1) |
| Product NDC | 11523-7340 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | OIL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 42.2; 63.3; 42.2; 25.32 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
