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MULTI-SYMPTOM ALLERGY - 62011-0056-3 - (diphenhydramine hydrochloride)

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Drug Information of MULTI-SYMPTOM ALLERGY

Product NDC: 62011-0056
Proprietary Name: MULTI-SYMPTOM ALLERGY
Non Proprietary Name: diphenhydramine hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   diphenhydramine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of MULTI-SYMPTOM ALLERGY

Product NDC: 62011-0056
Labeler Name: McKesson (Health Mart)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120214

Package Information of MULTI-SYMPTOM ALLERGY

Package NDC: 62011-0056-3
Package Description: 1 BOTTLE in 1 BOX (62011-0056-3) > 100 CAPSULE in 1 BOTTLE

NDC Information of MULTI-SYMPTOM ALLERGY

NDC Code 62011-0056-3
Proprietary Name MULTI-SYMPTOM ALLERGY
Package Description 1 BOTTLE in 1 BOX (62011-0056-3) > 100 CAPSULE in 1 BOTTLE
Product NDC 62011-0056
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson (Health Mart)
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of MULTI-SYMPTOM ALLERGY


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