| Product NDC: | 10956-813 |
| Proprietary Name: | REESES ONETAB COLD AND FLU |
| Non Proprietary Name: | ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10956-813 |
| Labeler Name: | REESE PHARMACEUTICAL CO. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100405 |
| Package NDC: | 10956-813-01 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (10956-813-01) > 30 TABLET in 1 BOTTLE, PLASTIC (10956-813-30) |
| NDC Code | 10956-813-01 |
| Proprietary Name | REESES ONETAB COLD AND FLU |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (10956-813-01) > 30 TABLET in 1 BOTTLE, PLASTIC (10956-813-30) |
| Product NDC | 10956-813 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN DIPHENHYDRAMINE HYDROCHLORIDE PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100405 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | REESE PHARMACEUTICAL CO. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 25; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |