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Coppertone Sensitive Skin - 11523-7300-1 - (Octinoxate, Octisalate, and Zinc Oxide)

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Drug Information of Coppertone Sensitive Skin

Product NDC: 11523-7300
Proprietary Name: Coppertone Sensitive Skin
Non Proprietary Name: Octinoxate, Octisalate, and Zinc Oxide
Active Ingredient(s): 85.2; 56.8; 164.72    mg/mL; mg/mL; mg/mL & nbsp;   Octinoxate, Octisalate, and Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Coppertone Sensitive Skin

Product NDC: 11523-7300
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 Information of Coppertone Sensitive Skin

Package NDC: 11523-7300-1
Package Description: 30 mL in 1 TUBE (11523-7300-1)

NDC Information of Coppertone Sensitive Skin

NDC Code 11523-7300-1
Proprietary Name Coppertone Sensitive Skin
Package Description 30 mL in 1 TUBE (11523-7300-1)
Product NDC 11523-7300
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate, and Zinc Oxide
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 OCTINOXATE; OCTISALATE; ZINC OXIDE
Strength Number 85.2; 56.8; 164.72
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Coppertone Sensitive Skin


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