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CHAPSTICK ULTRA SPF 30 - 0573-1940-50 - (OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM)

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Drug Information of CHAPSTICK ULTRA SPF 30

Product NDC: 0573-1940
Proprietary Name: CHAPSTICK ULTRA SPF 30
Non Proprietary Name: OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM
Active Ingredient(s): 75; 50; 70; 50; 300    mg/g; mg/g; mg/g; mg/g; mg/g & nbsp;   OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM
Administration Route(s): TOPICAL
Dosage Form(s): STICK
Coding System: National Drug Codes(NDC)

Labeler Information of CHAPSTICK ULTRA SPF 30

Product NDC: 0573-1940
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040130

Package Information of CHAPSTICK ULTRA SPF 30

Package NDC: 0573-1940-50
Package Description: 4 g in 1 CYLINDER (0573-1940-50)

NDC Information of CHAPSTICK ULTRA SPF 30

NDC Code 0573-1940-50
Proprietary Name CHAPSTICK ULTRA SPF 30
Package Description 4 g in 1 CYLINDER (0573-1940-50)
Product NDC 0573-1940
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, PETROLATUM
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20040130
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Pfizer Consumer Healthcare
Substance Name OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; PETROLATUM
Strength Number 75; 50; 70; 50; 300
Strength Unit mg/g; mg/g; mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of CHAPSTICK ULTRA SPF 30


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