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KALI CARBONICUM
KALI CARBONICUM - 10191-1665-2 - (POTASSIUM CARBONATE)
Drug Information of KALI CARBONICUM
| Product NDC: | 10191-1665 |
| Proprietary Name: | KALI CARBONICUM |
| Non Proprietary Name: | POTASSIUM CARBONATE |
| Active Ingredient(s): | 6 [hp_C]/1 & nbsp; POTASSIUM CARBONATE |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KALI CARBONICUM
| Product NDC: | 10191-1665 |
| Labeler Name: | REMEDY MAKERS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111208 |
Package Information of KALI CARBONICUM
| Package NDC: | 10191-1665-2 |
| Package Description: | 145 PELLET in 1 VIAL, GLASS (10191-1665-2) |
NDC Information of KALI CARBONICUM
| NDC Code | 10191-1665-2 |
| Proprietary Name | KALI CARBONICUM |
| Package Description | 145 PELLET in 1 VIAL, GLASS (10191-1665-2) |
| Product NDC | 10191-1665 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | POTASSIUM CARBONATE |
| Dosage Form Name | PELLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20111208 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | REMEDY MAKERS |
| Substance Name | POTASSIUM CARBONATE |
| Strength Number | 6 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
