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REESES ONETAB ALLERGY AND SINUS - 10956-812-01 - (ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE)

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Drug Information of REESES ONETAB ALLERGY AND SINUS

Product NDC: 10956-812
Proprietary Name: REESES ONETAB ALLERGY AND SINUS
Non Proprietary Name: ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE
Active Ingredient(s): 650; 25; 10    mg/1; mg/1; mg/1 & nbsp;   ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of REESES ONETAB ALLERGY AND SINUS

Product NDC: 10956-812
Labeler Name: REESE PHARMACEUTICAL CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100405

Package Information of REESES ONETAB ALLERGY AND SINUS

Package NDC: 10956-812-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (10956-812-01) > 30 TABLET in 1 BOTTLE, PLASTIC (10956-812-30)

NDC Information of REESES ONETAB ALLERGY AND SINUS

NDC Code 10956-812-01
Proprietary Name REESES ONETAB ALLERGY AND SINUS
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (10956-812-01) > 30 TABLET in 1 BOTTLE, PLASTIC (10956-812-30)
Product NDC 10956-812
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100405
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name REESE PHARMACEUTICAL CO.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 650; 25; 10
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of REESES ONETAB ALLERGY AND SINUS


General Information