Product NDC: | 53799-261 |
Proprietary Name: | Mucus Relief |
Non Proprietary Name: | Antimony Pentasulfide and Polygala Senega Root and Potassium Iodide |
Active Ingredient(s): | 12; 8; 12 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL & nbsp; Antimony Pentasulfide and Polygala Senega Root and Potassium Iodide |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53799-261 |
Labeler Name: | Similasan AG |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130630 |
Package NDC: | 53799-261-25 |
Package Description: | 118 mL in 1 BOTTLE, GLASS (53799-261-25) |
NDC Code | 53799-261-25 |
Proprietary Name | Mucus Relief |
Package Description | 118 mL in 1 BOTTLE, GLASS (53799-261-25) |
Product NDC | 53799-261 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Antimony Pentasulfide and Polygala Senega Root and Potassium Iodide |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20130630 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Similasan AG |
Substance Name | ANTIMONY PENTASULFIDE; POLYGALA SENEGA ROOT; POTASSIUM IODIDE |
Strength Number | 12; 8; 12 |
Strength Unit | [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL |
Pharmaceutical Classes |