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Rx Act sinus and allergy PE - 37808-358-62 - (Chlorpheniramine maleate, Phenylephrine HCl)

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Drug Information of Rx Act sinus and allergy PE

Product NDC: 37808-358
Proprietary Name: Rx Act sinus and allergy PE
Non Proprietary Name: Chlorpheniramine maleate, Phenylephrine HCl
Active Ingredient(s): 4; 10    mg/1; mg/1 & nbsp;   Chlorpheniramine maleate, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act sinus and allergy PE

Product NDC: 37808-358
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100521

Package Information of Rx Act sinus and allergy PE

Package NDC: 37808-358-62
Package Description: 1 BLISTER PACK in 1 CARTON (37808-358-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Rx Act sinus and allergy PE

NDC Code 37808-358-62
Proprietary Name Rx Act sinus and allergy PE
Package Description 1 BLISTER PACK in 1 CARTON (37808-358-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 37808-358
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorpheniramine maleate, Phenylephrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100521
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 4; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Rx Act sinus and allergy PE


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