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up and up allergy relief - 11673-690-78 - (Diphenhydramine Hydrochloride)

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Drug Information of up and up allergy relief

Product NDC: 11673-690
Proprietary Name: up and up allergy relief
Non Proprietary Name: Diphenhydramine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of up and up allergy relief

Product NDC: 11673-690
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090612

Package Information of up and up allergy relief

Package NDC: 11673-690-78
Package Description: 1 BOTTLE in 1 CARTON (11673-690-78) > 100 TABLET in 1 BOTTLE

NDC Information of up and up allergy relief

NDC Code 11673-690-78
Proprietary Name up and up allergy relief
Package Description 1 BOTTLE in 1 CARTON (11673-690-78) > 100 TABLET in 1 BOTTLE
Product NDC 11673-690
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up allergy relief


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