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Scot-Tussin Original SF Multi-Symptom - 0372-0004-04 - (Acetominophen, Phenylephrine Hydrochloride and Pheniramine Maleate)

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Drug Information of Scot-Tussin Original SF Multi-Symptom

Product NDC: 0372-0004
Proprietary Name: Scot-Tussin Original SF Multi-Symptom
Non Proprietary Name: Acetominophen, Phenylephrine Hydrochloride and Pheniramine Maleate
Active Ingredient(s): 160; 4; 4    mg/5mL; mg/5mL; mg/5mL & nbsp;   Acetominophen, Phenylephrine Hydrochloride and Pheniramine Maleate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Scot-Tussin Original SF Multi-Symptom

Product NDC: 0372-0004
Labeler Name: SCOT-TUSSIN Pharmacal Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19561201

Package Information of Scot-Tussin Original SF Multi-Symptom

Package NDC: 0372-0004-04
Package Description: 118 mL in 1 BOTTLE (0372-0004-04)

NDC Information of Scot-Tussin Original SF Multi-Symptom

NDC Code 0372-0004-04
Proprietary Name Scot-Tussin Original SF Multi-Symptom
Package Description 118 mL in 1 BOTTLE (0372-0004-04)
Product NDC 0372-0004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetominophen, Phenylephrine Hydrochloride and Pheniramine Maleate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19561201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SCOT-TUSSIN Pharmacal Co., Inc.
Substance Name ACETAMINOPHEN; PHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 160; 4; 4
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Scot-Tussin Original SF Multi-Symptom


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