KALI CARBONICUM
- Product NDC
- 10191-1665
- 11-digit product format
- 101911665
- Labeler code
- 10191
- Product ID
- 10191-1665_beff73bc-c5b8-4b95-8c8e-2c61a2067cb6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM CARBONATE
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- REMEDY MAKERS
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-12-08
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CARBONATE
- Active strength
- 6 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10191-1665-2 | KALI CARBONICUM | 145 in 1 VIAL, GLASS | PELLET | 145 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1665 | KALI CARBONICUM (POTASSIUM CARBONATE) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111228_ad82631d-7c0e-4d54-b1dc-a33c4b5f119e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1665-2 | 10191166502 | 145 in 1 VIAL, GLASS | Historical |