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Coppertone ultraGUARD - 11523-7323-2 - (Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone)

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Drug Information of Coppertone ultraGUARD

Product NDC: 11523-7323
Proprietary Name: Coppertone ultraGUARD
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Active Ingredient(s): 26.03; 86.76; 43.38; 34.7; 43.38    mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Coppertone ultraGUARD

Product NDC: 11523-7323
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 ultraGUARD

Package NDC: 11523-7323-2
Package Description: 222 mL in 1 BOTTLE, SPRAY (11523-7323-2)

NDC Information of Coppertone ultraGUARD

NDC Code 11523-7323-2
Proprietary Name Coppertone ultraGUARD
Package Description 222 mL in 1 BOTTLE, SPRAY (11523-7323-2)
Product NDC 11523-7323
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 19990521
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Schering-Plough HealthCare Products, Inc.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 26.03; 86.76; 43.38; 34.7; 43.38
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Coppertone ultraGUARD


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