SULPHUR
- Product NDC
- 60512-1047
- 11-digit product format
- 605121047
- Labeler code
- 60512
- Product ID
- 60512-1047_8c12e5a9-ceec-457b-a30c-690b132bc11f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULPHUR
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1995-10-11
- Marketing end
- 0000-00-00
- Substance
- SULFUR
- Active strength
- 1 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60512-1047 | SULPHUR PELLET [HOMEOLAB USA INC] | 1 | Legacy NDC | 20140514_1468698c-066f-4972-8bf3-6ace9f6c66c5.zip |