| Product NDC: | 0031-2247 |
| Proprietary Name: | CHILDRENS DIMETAPP NIGHTTIME COLD AND CONGESTION |
| Non Proprietary Name: | diphenhydramine HCl, phenylephrine HCl |
| Active Ingredient(s): | 6.25; 2.5 mg/5mL; mg/5mL & nbsp; diphenhydramine HCl, phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0031-2247 |
| Labeler Name: | Richmond Division of Wyeth LLC, a subsidiary of Pfizer Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20071101 |
| Package NDC: | 0031-2247-13 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-2247-13) > 118 mL in 1 BOTTLE |
| NDC Code | 0031-2247-13 |
| Proprietary Name | CHILDRENS DIMETAPP NIGHTTIME COLD AND CONGESTION |
| Package Description | 1 BOTTLE in 1 CARTON (0031-2247-13) > 118 mL in 1 BOTTLE |
| Product NDC | 0031-2247 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine HCl, phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20071101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth LLC, a subsidiary of Pfizer Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 6.25; 2.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |