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Day Time Cold Multi-Symptom
Day Time Cold Multi-Symptom - 55910-560-08 - (Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr)
Drug Information of Day Time Cold Multi-Symptom
| Product NDC: | 55910-560 |
| Proprietary Name: | Day Time Cold Multi-Symptom |
| Non Proprietary Name: | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Active Ingredient(s): | 325; 10; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Day Time Cold Multi-Symptom
| Product NDC: | 55910-560 |
| Labeler Name: | DOLGENCORP, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080329 |
Package Information of Day Time Cold Multi-Symptom
| Package NDC: | 55910-560-08 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (55910-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Day Time Cold Multi-Symptom
| NDC Code | 55910-560-08 |
| Proprietary Name | Day Time Cold Multi-Symptom |
| Package Description | 1 BLISTER PACK in 1 CARTON (55910-560-08) > 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 55910-560 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenylephrine HCl and Dextromethorphan HBr |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20080329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DOLGENCORP, LLC |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
