SULPHUR
- Product NDC
- 10191-1578
- 11-digit product format
- 101911578
- Labeler code
- 10191
- Product ID
- 10191-1578_b47d449e-7bb3-4708-8ece-fd498725f9a7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- REMEDY MAKERS
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1998-12-08
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 6 [hp_X]/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 |
|---|
| 10191-1578-2 | SULPHUR | 137 in 1 VIAL, GLASS | PELLET | 137 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1578 | SULPHUR (SULFUR) PELLET [REMEDY MAKERS] | 1 | Legacy NDC, 1 package rows | 20111102_b7c44b08-824a-4365-82f8-32997e1fcff6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1578-2 | 10191157802 | 137 in 1 VIAL, GLASS | Historical |