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PRO-CHLO
PRO-CHLO - 66594-321-01 - (Chlophedianol Hydrochloride, Phenylephrine Hydrochloride, Pyrilamine Maleate)
Drug Information of PRO-CHLO
| Product NDC: | 66594-321 |
| Proprietary Name: | PRO-CHLO |
| Non Proprietary Name: | Chlophedianol Hydrochloride, Phenylephrine Hydrochloride, Pyrilamine Maleate |
| Active Ingredient(s): | 12.5; 5; 12.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Chlophedianol Hydrochloride, Phenylephrine Hydrochloride, Pyrilamine Maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRO-CHLO
| Product NDC: | 66594-321 |
| Labeler Name: | Pro-Pharma, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111212 |
Package Information of PRO-CHLO
| Package NDC: | 66594-321-01 |
| Package Description: | 30 mL in 1 BOTTLE (66594-321-01) |
NDC Information of PRO-CHLO
| NDC Code | 66594-321-01 |
| Proprietary Name | PRO-CHLO |
| Package Description | 30 mL in 1 BOTTLE (66594-321-01) |
| Product NDC | 66594-321 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlophedianol Hydrochloride, Phenylephrine Hydrochloride, Pyrilamine Maleate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111212 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pro-Pharma, LLC |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE |
| Strength Number | 12.5; 5; 12.5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
