| Product NDC: | 0485-0096 |
| Proprietary Name: | ED CHLORPED D |
| Non Proprietary Name: | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 2; 5 mg/mL; mg/mL & nbsp; CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0485-0096 |
| Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110601 |
| Package NDC: | 0485-0096-02 |
| Package Description: | 60 mL in 1 BOTTLE, DROPPER (0485-0096-02) |
| NDC Code | 0485-0096-02 |
| Proprietary Name | ED CHLORPED D |
| Package Description | 60 mL in 1 BOTTLE, DROPPER (0485-0096-02) |
| Product NDC | 0485-0096 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
| Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |