| Product NDC: | 63029-404 |
| Proprietary Name: | Little Colds Multi Symptom Cold |
| Non Proprietary Name: | Acetaminophen and Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Active Ingredient(s): | 80; 2.5; 1.25 mg/mL; mg/mL; mg/mL & nbsp; Acetaminophen and Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63029-404 |
| Labeler Name: | Medtech Products Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
| Package NDC: | 63029-404-01 |
| Package Description: | 1 BOTTLE, DROPPER in 1 BOX (63029-404-01) > 30 mL in 1 BOTTLE, DROPPER |
| NDC Code | 63029-404-01 |
| Proprietary Name | Little Colds Multi Symptom Cold |
| Package Description | 1 BOTTLE, DROPPER in 1 BOX (63029-404-01) > 30 mL in 1 BOTTLE, DROPPER |
| Product NDC | 63029-404 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Medtech Products Inc. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 80; 2.5; 1.25 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |