Product NDC: | 0924-0140 |
Proprietary Name: | PhysiciansCare Cold and Cough |
Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 15; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0924-0140 |
Labeler Name: | Acme United Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120128 |
Package NDC: | 0924-0140-01 |
Package Description: | 50 PACKET in 1 CARTON (0924-0140-01) > 2 TABLET, FILM COATED in 1 PACKET |
NDC Code | 0924-0140-01 |
Proprietary Name | PhysiciansCare Cold and Cough |
Package Description | 50 PACKET in 1 CARTON (0924-0140-01) > 2 TABLET, FILM COATED in 1 PACKET |
Product NDC | 0924-0140 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120128 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Acme United Corporation |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 15; 200; 5 |
Strength Unit | mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |