| 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 |