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Medicated Pad - 50730-7549-1 - (witch hazel)

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Drug Information of Medicated Pad

Product NDC: 50730-7549
Proprietary Name: Medicated Pad
Non Proprietary Name: witch hazel
Active Ingredient(s): .5    mL/mL & nbsp;   witch hazel
Administration Route(s): RECTAL; TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Medicated Pad

Product NDC: 50730-7549
Labeler Name: H and P Industries, Inc. dba Triad Group
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070201

Package Information of Medicated Pad

Package NDC: 50730-7549-1
Package Description: 100 APPLICATOR in 1 JAR (50730-7549-1) > 2.5 mL in 1 APPLICATOR

NDC Information of Medicated Pad

NDC Code 50730-7549-1
Proprietary Name Medicated Pad
Package Description 100 APPLICATOR in 1 JAR (50730-7549-1) > 2.5 mL in 1 APPLICATOR
Product NDC 50730-7549
Product Type Name HUMAN OTC DRUG
Non Proprietary Name witch hazel
Dosage Form Name SOLUTION
Route Name RECTAL; TOPICAL
Start Marketing Date 20070201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H and P Industries, Inc. dba Triad Group
Substance Name WITCH HAZEL
Strength Number .5
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Medicated Pad


General Information