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Rx Act Tussin CF - 37808-516-26 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of Rx Act Tussin CF

Product NDC: 37808-516
Proprietary Name: Rx Act Tussin CF
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 10; 100; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act Tussin CF

Product NDC: 37808-516
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19960718

Package Information of Rx Act Tussin CF

Package NDC: 37808-516-26
Package Description: 1 BOTTLE in 1 CARTON (37808-516-26) > 118 mL in 1 BOTTLE

NDC Information of Rx Act Tussin CF

NDC Code 37808-516-26
Proprietary Name Rx Act Tussin CF
Package Description 1 BOTTLE in 1 CARTON (37808-516-26) > 118 mL in 1 BOTTLE
Product NDC 37808-516
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19960718
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10; 100; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Rx Act Tussin CF


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