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Day Time Cold Multi-Symptom Severe
Day Time Cold Multi-Symptom Severe - 55910-035-08 - (Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin)
Drug Information of Day Time Cold Multi-Symptom Severe
| Product NDC: | 55910-035 |
| Proprietary Name: | Day Time Cold Multi-Symptom Severe |
| Non Proprietary Name: | Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Active Ingredient(s): | 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Day Time Cold Multi-Symptom Severe
| Product NDC: | 55910-035 |
| Labeler Name: | DOLGENCORP, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050804 |
Package Information of Day Time Cold Multi-Symptom Severe
| Package NDC: | 55910-035-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (55910-035-08) > 24 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Day Time Cold Multi-Symptom Severe
| NDC Code | 55910-035-08 |
| Proprietary Name | Day Time Cold Multi-Symptom Severe |
| Package Description | 1 BLISTER PACK in 1 CARTON (55910-035-08) > 24 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 55910-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050804 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DOLGENCORP, LLC |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
