Product NDC: | 11523-7218 |
Proprietary Name: | Coppertone UltraGuard |
Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Oxybenzone |
Active Ingredient(s): | 16.89; 84.47; 42.235; 25.34 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Homosalate, Octisalate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11523-7218 |
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 NDC: | 11523-7218-1 |
Package Description: | 177 mL in 1 CAN (11523-7218-1) |
NDC Code | 11523-7218-1 |
Proprietary Name | Coppertone UltraGuard |
Package Description | 177 mL in 1 CAN (11523-7218-1) |
Product NDC | 11523-7218 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Oxybenzone |
Dosage Form Name | AEROSOL, SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 19990521 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | MSD Consumer Care, Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
Strength Number | 16.89; 84.47; 42.235; 25.34 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |