SULPHUR
- Product NDC
- 10191-1589
- 11-digit product format
- 101911589
- Labeler code
- 10191
- Product ID
- 10191-1589_63494dd2-60c5-422a-bc8d-dbf498cd16fa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2002-09-09
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 30 [hp_C]/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10191-1589-2 | SULPHUR | 152 in 1 VIAL, GLASS | PELLET | 152 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1589 | SULPHUR (SULFUR) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20100402_6307241a-d3fa-4b97-bb90-509901314b12.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1589-2 | 10191158902 | 152 in 1 VIAL, GLASS | Historical |