SULPHUR
- Product NDC
- 10191-1585
- 11-digit product format
- 101911585
- Labeler code
- 10191
- Product ID
- 10191-1585_21ccc2d5-c363-443e-9b43-2c5e1ae04e28
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- PELLET
- Route
- SUBLINGUAL
- Labeler
- Remedy Makers
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1998-12-15
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 6 [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 |
|---|
| 10191-1585-2 | SULPHUR | 151 in 1 VIAL, GLASS | PELLET | 151 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10191-1585 | SULPHUR (SULFUR) PELLET [REMEDY MAKERS] | 2 | Legacy NDC, 1 package rows | 20100312_f0cbf8e3-6601-4955-a738-d6045a28835d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10191-1585-2 | 10191158502 | 151 in 1 VIAL, GLASS | Historical |