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