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THE QUEEN ROSE - 55885-010-01 - (WITCH HAZEL)

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Drug Information of THE QUEEN ROSE

Product NDC: 55885-010
Proprietary Name: THE QUEEN ROSE
Non Proprietary Name: WITCH HAZEL
Active Ingredient(s): .005    mg/5mL & nbsp;   WITCH HAZEL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of THE QUEEN ROSE

Product NDC: 55885-010
Labeler Name: LaLa Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121201

Package Information of THE QUEEN ROSE

Package NDC: 55885-010-01
Package Description: 5 mL in 1 CARTON (55885-010-01)

NDC Information of THE QUEEN ROSE

NDC Code 55885-010-01
Proprietary Name THE QUEEN ROSE
Package Description 5 mL in 1 CARTON (55885-010-01)
Product NDC 55885-010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name WITCH HAZEL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20121201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name LaLa Co., Ltd.
Substance Name WITCH HAZEL
Strength Number .005
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of THE QUEEN ROSE


General Information