Sulphur
- Product NDC
- 0220-4820
- 11-digit product format
- 002204820
- Labeler code
- 0220
- Product ID
- 0220-4820_f52c0d73-6bd9-6378-e053-2995a90aebc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- SULFUR
- Active strength
- 1 [hp_M]/[hp_M]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sulphur
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 1 [hp_M]/[hp_M] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-4820-41 | Sulphur | 1 [hp_M] in 1 TUBE | PELLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-4820 | SULPHUR (SULFUR) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230222_8696b1c1-7329-3eed-e053-2991aa0a9617.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-4820-41 | 00220482041 | 1 [hp_M] in 1 TUBE (0220-4820-41) | 1983-03-03 | 0000-00-00 | No | No | Current |