Product NDC: | 11523-7141 |
Proprietary Name: | Coppertone oil free faces Sunscreen |
Non Proprietary Name: | avobenzone, homosalate, octisalate, octocrylene, and oxybenzone |
Active Ingredient(s): | 20.7; 134.55; 51.75; 20.7; 41.4 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) |
Product NDC: | 11523-7141 |
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: | 11523-7141-1 |
Package Description: | 88 mL in 1 BOTTLE, PLASTIC (11523-7141-1) |
NDC Code | 11523-7141-1 |
Proprietary Name | Coppertone oil free faces Sunscreen |
Package Description | 88 mL in 1 BOTTLE, PLASTIC (11523-7141-1) |
Product NDC | 11523-7141 |
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 | MSD Consumer Care, Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 20.7; 134.55; 51.75; 20.7; 41.4 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |