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Scarlight MD - 64269-9902-7 - (HYDROQUINONE)

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Drug Information of Scarlight MD

Product NDC: 64269-9902
Proprietary Name: Scarlight MD
Non Proprietary Name: HYDROQUINONE
Active Ingredient(s): 20    mg/mL & nbsp;   HYDROQUINONE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Scarlight MD

Product NDC: 64269-9902
Labeler Name: Scarguard Labs, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part358
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20021101

Package Information of Scarlight MD

Package NDC: 64269-9902-7
Package Description: 15 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-7)

NDC Information of Scarlight MD

NDC Code 64269-9902-7
Proprietary Name Scarlight MD
Package Description 15 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-7)
Product NDC 64269-9902
Product Type Name HUMAN OTC DRUG
Non Proprietary Name HYDROQUINONE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20021101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Scarguard Labs, LLC
Substance Name HYDROQUINONE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Scarlight MD


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