Product NDC: | 50991-222 |
Proprietary Name: | Poly Hist PD |
Non Proprietary Name: | Thonzylamine Hydrochloride and Chlophedianol Hydrochloride |
Active Ingredient(s): | 6.25; 6.25 mg/mL; mg/mL & nbsp; Thonzylamine Hydrochloride and Chlophedianol Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50991-222 |
Labeler Name: | Poly Pharmaceuticals, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130701 |
Package NDC: | 50991-222-45 |
Package Description: | 45 mL in 1 BOTTLE (50991-222-45) |
NDC Code | 50991-222-45 |
Proprietary Name | Poly Hist PD |
Package Description | 45 mL in 1 BOTTLE (50991-222-45) |
Product NDC | 50991-222 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Thonzylamine Hydrochloride and Chlophedianol Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Poly Pharmaceuticals, Inc. |
Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; THONZYLAMINE HYDROCHLORIDE |
Strength Number | 6.25; 6.25 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |