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ReCreate Foundation - 51060-001-29 - (Octinoxate, Octisalate, and Oxybenzone)

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Drug Information of ReCreate Foundation

Product NDC: 51060-001
Proprietary Name: ReCreate Foundation
Non Proprietary Name: Octinoxate, Octisalate, and Oxybenzone
Active Ingredient(s): 2.2125; 1.18; .59    mL/29.5mL; mL/29.5mL; mL/29.5mL & nbsp;   Octinoxate, Octisalate, and Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ReCreate Foundation

Product NDC: 51060-001
Labeler Name: Tarte Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100601

Package Information of ReCreate Foundation

Package NDC: 51060-001-29
Package Description: 1 BOTTLE, PUMP in 1 CARTON (51060-001-29) > 29.5 mL in 1 BOTTLE, PUMP

NDC Information of ReCreate Foundation

NDC Code 51060-001-29
Proprietary Name ReCreate Foundation
Package Description 1 BOTTLE, PUMP in 1 CARTON (51060-001-29) > 29.5 mL in 1 BOTTLE, PUMP
Product NDC 51060-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate, and Oxybenzone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Tarte Inc
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 2.2125; 1.18; .59
Strength Unit mL/29.5mL; mL/29.5mL; mL/29.5mL
Pharmaceutical Classes

Complete Information of ReCreate Foundation


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