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Blue Lizard Face - 0316-2055-40 - (Sunscreen)

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Drug Information of Blue Lizard Face

Product NDC: 0316-2055
Proprietary Name: Blue Lizard Face
Non Proprietary Name: Sunscreen
Active Ingredient(s): 55; 80    mg/g; mg/g & nbsp;   Sunscreen
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Blue Lizard Face

Product NDC: 0316-2055
Labeler Name: Crown Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100406

Package Information of Blue Lizard Face

Package NDC: 0316-2055-40
Package Description: 141.7 g in 1 BOTTLE, PLASTIC (0316-2055-40)

NDC Information of Blue Lizard Face

NDC Code 0316-2055-40
Proprietary Name Blue Lizard Face
Package Description 141.7 g in 1 BOTTLE, PLASTIC (0316-2055-40)
Product NDC 0316-2055
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sunscreen
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100406
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Crown Laboratories
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 55; 80
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Blue Lizard Face


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