SULPHUR
- Product NDC
- 15631-2322
- 11-digit product format
- 156312322
- Labeler code
- 15631
- Product ID
- 15631-2322_fa4fe270-9cdf-435c-a611-5cf511a5be4f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULPHUR
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-04-26
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 1 [hp_X]/g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 15631-2322 | SULPHUR GEL [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC] | 1 | Legacy NDC, 8 package rows | 20160509_824dc045-e4bc-4956-85a9-b921dfcc53ce.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 15631-2322-0 | 15631232200 | 50 g in 1 CONTAINER | 50 g | Historical |
| 15631-2322-1 | 15631232201 | 1 in 1 CONTAINER | | Historical |
| 15631-2322-2 | 15631232202 | 200 g in 1 CONTAINER | 200 g | Historical |
| 15631-2322-3 | 15631232203 | 500 g in 1 CONTAINER | 500 g | Historical |