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Coppertone KIDS - 11523-7301-1 - (Octinoxate, Octisalate, and Zinc Oxide)

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Drug Information of Coppertone KIDS

Product NDC: 11523-7301
Proprietary Name: Coppertone KIDS
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 KIDS

Product NDC: 11523-7301
Labeler Name: Schering-Plough HealthCare Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19990521

Package Information of Coppertone KIDS

Package NDC: 11523-7301-1
Package Description: 237 mL in 1 BOTTLE, PLASTIC (11523-7301-1)

NDC Information of Coppertone KIDS

NDC Code 11523-7301-1
Proprietary Name Coppertone KIDS
Package Description 237 mL in 1 BOTTLE, PLASTIC (11523-7301-1)
Product NDC 11523-7301
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 Schering-Plough HealthCare Products, 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 KIDS


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