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Cold Relief Severe Pain Cough
Cold Relief Severe Pain Cough - 52904-456-02 - (Acetaminophen,Guaifenesin, Phenylephrine HCl, Dextromethorphan Hydrobromide)
Drug Information of Cold Relief Severe Pain Cough
| Product NDC: | 52904-456 |
| Proprietary Name: | Cold Relief Severe Pain Cough |
| Non Proprietary Name: | Acetaminophen,Guaifenesin, Phenylephrine HCl, Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 325; 15; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen,Guaifenesin, Phenylephrine HCl, Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cold Relief Severe Pain Cough
| Product NDC: | 52904-456 |
| Labeler Name: | Select Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121015 |
Package Information of Cold Relief Severe Pain Cough
| Package NDC: | 52904-456-02 |
| Package Description: | 2 TABLET in 1 PACKET (52904-456-02) |
NDC Information of Cold Relief Severe Pain Cough
| NDC Code | 52904-456-02 |
| Proprietary Name | Cold Relief Severe Pain Cough |
| Package Description | 2 TABLET in 1 PACKET (52904-456-02) |
| Product NDC | 52904-456 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen,Guaifenesin, Phenylephrine HCl, Dextromethorphan Hydrobromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Select 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 |
