| Product NDC: | 11523-7347 |
| Proprietary Name: | Coppertone Tanning Sunscreen |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Active Ingredient(s): | 20; 100; 40.5; 50 mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11523-7347 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121101 |
| Package NDC: | 11523-7347-1 |
| Package Description: | 170 g in 1 CAN (11523-7347-1) |
| NDC Code | 11523-7347-1 |
| Proprietary Name | Coppertone Tanning Sunscreen |
| Package Description | 170 g in 1 CAN (11523-7347-1) |
| Product NDC | 11523-7347 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, and Octocrylene |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 20; 100; 40.5; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |