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 |