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daytime cold relief
daytime cold relief - 11822-0308-1 - (Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of daytime cold relief
| Product NDC: | 11822-0308 |
| Proprietary Name: | daytime cold relief |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 325; 10; 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) |
Labeler Information of daytime cold relief
| Product NDC: | 11822-0308 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071022 |
Package Information of daytime cold relief
| Package NDC: | 11822-0308-1 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (11822-0308-1) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of daytime cold relief
| NDC Code | 11822-0308-1 |
| Proprietary Name | daytime cold relief |
| Package Description | 2 BLISTER PACK in 1 CARTON (11822-0308-1) > 12 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 11822-0308 |
| 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 | 20071022 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rite Aid Corporation |
| 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 |
