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Coppertone ultraGUARD Sunscreen - 11523-7313-1 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)

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Drug Information of Coppertone ultraGUARD Sunscreen

Product NDC: 11523-7313
Proprietary Name: Coppertone ultraGUARD Sunscreen
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Active Ingredient(s): 30.06; 150.3; 50.1; 100.2; 60.12    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)

Labeler Information of Coppertone ultraGUARD Sunscreen

Product NDC: 11523-7313
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 ultraGUARD Sunscreen

Package NDC: 11523-7313-1
Package Description: 177 mL in 1 BOTTLE, PLASTIC (11523-7313-1)

NDC Information of Coppertone ultraGUARD Sunscreen

NDC Code 11523-7313-1
Proprietary Name Coppertone ultraGUARD Sunscreen
Package Description 177 mL in 1 BOTTLE, PLASTIC (11523-7313-1)
Product NDC 11523-7313
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 30.06; 150.3; 50.1; 100.2; 60.12
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Coppertone ultraGUARD Sunscreen


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