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Mustela SPF 50 - 64768-2920-1 - (TITANIUM DIOXIDE and ZINC OXIDE)

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Drug Information of Mustela SPF 50

Product NDC: 64768-2920
Proprietary Name: Mustela SPF 50
Non Proprietary Name: TITANIUM DIOXIDE and ZINC OXIDE
Active Ingredient(s): 60; 47    mg/mL; mg/mL & nbsp;   TITANIUM DIOXIDE and ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mustela SPF 50

Product NDC: 64768-2920
Labeler Name: Expanscience Laboratories d/b/a Mustela
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130215

Package Information of Mustela SPF 50

Package NDC: 64768-2920-1
Package Description: 1 TUBE in 1 CARTON (64768-2920-1) > 100 mL in 1 TUBE

NDC Information of Mustela SPF 50

NDC Code 64768-2920-1
Proprietary Name Mustela SPF 50
Package Description 1 TUBE in 1 CARTON (64768-2920-1) > 100 mL in 1 TUBE
Product NDC 64768-2920
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE and ZINC OXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130215
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Expanscience Laboratories d/b/a Mustela
Substance Name TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 60; 47
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Mustela SPF 50


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