Product NDC: | 11523-7032 |
Proprietary Name: | Coppertone Sport Sunscreen |
Non Proprietary Name: | homosalate, octisalate, octinoxate, and oxybenzone |
Active Ingredient(s): | 80; 75; 50; 60 mg/g; mg/g; mg/g; mg/g & nbsp; homosalate, octisalate, octinoxate, and oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11523-7032 |
Labeler Name: | MSD Consumer Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19990521 |
Package NDC: | 11523-7032-1 |
Package Description: | 1 TUBE in 1 BLISTER PACK (11523-7032-1) > 17 g in 1 TUBE |
NDC Code | 11523-7032-1 |
Proprietary Name | Coppertone Sport Sunscreen |
Package Description | 1 TUBE in 1 BLISTER PACK (11523-7032-1) > 17 g in 1 TUBE |
Product NDC | 11523-7032 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | homosalate, octisalate, octinoxate, and oxybenzone |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 19990521 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | MSD Consumer Care, Inc. |
Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 80; 75; 50; 60 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |