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up and up anti itch - 11673-369-64 - (Hydrocortisone)

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Drug Information of up and up anti itch

Product NDC: 11673-369
Proprietary Name: up and up anti itch
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 1    g/100g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of up and up anti itch

Product NDC: 11673-369
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110317

Package Information of up and up anti itch

Package NDC: 11673-369-64
Package Description: 1 TUBE in 1 CARTON (11673-369-64) > 28 g in 1 TUBE

NDC Information of up and up anti itch

NDC Code 11673-369-64
Proprietary Name up and up anti itch
Package Description 1 TUBE in 1 CARTON (11673-369-64) > 28 g in 1 TUBE
Product NDC 11673-369
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110317
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Target Corporation
Substance Name HYDROCORTISONE
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of up and up anti itch


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