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Coppertone ultraGUARD Sunscreen
Coppertone ultraGUARD Sunscreen - 11523-7318-1 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)
Drug Information of Coppertone ultraGUARD Sunscreen
| Product NDC: | 11523-7318 |
| Proprietary Name: | Coppertone ultraGUARD Sunscreen |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | 30.06; 150.3; 50.1; 100.2; 60.12 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Coppertone ultraGUARD Sunscreen
| Product NDC: | 11523-7318 |
| Labeler Name: | Schering-Plough HealthCare Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19990521 |
Package Information of Coppertone ultraGUARD Sunscreen
| Package NDC: | 11523-7318-1 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (11523-7318-1) |
NDC Information of Coppertone ultraGUARD Sunscreen
| NDC Code | 11523-7318-1 |
| Proprietary Name | Coppertone ultraGUARD Sunscreen |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (11523-7318-1) |
| Product NDC | 11523-7318 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19990521 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Schering-Plough HealthCare Products, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30.06; 150.3; 50.1; 100.2; 60.12 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
