| 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 |