Natrum sulphuricum
- Product NDC
- 0220-3635
- 11-digit product format
- 002203635
- Labeler code
- 0220
- Product ID
- 0220-3635_0a1f9be1-3bb3-be83-e063-6394a90a8b2f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM SULFATE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- SODIUM SULFATE
- Active strength
- 12 [hp_C]/12[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Natrum sulphuricum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM SULFATE | 12 [hp_C]/12[hp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0YPR65R21J |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-3635-41 | Natrum sulphuricum | 12 [hp_C] in 1 TUBE | PELLET | 12 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-3635 | NATRUM SULPHURICUM (SODIUM SULFATE ) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231115_86481c93-4c94-2dd1-e053-2a91aa0ae99f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-3635-41 | 00220363541 | 12 [hp_C] in 1 TUBE (0220-3635-41) | 1983-03-03 | 0000-00-00 | No | No | Current |