Natrum Sulphuricum
- Product NDC
- 71753-8011
- 11-digit product format
- 717538011
- Labeler code
- 71753
- Product ID
- 71753-8011_2cc44cf3-5cfb-4a35-a8ea-06831753548a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Natrum Sulphuricum
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Ratis, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-09-30
- Marketing end
- 2025-10-26
- Substance
- SODIUM SULFATE
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71753-8011 | NATRUM SULPHURICUM SPRAY [RATIS, LLC] | 2 | Legacy NDC | 20220121_ca0e0398-3e97-4e6c-a419-cdfb6f85bce6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71753-8011-1 | 71753801101 | 30 mL in 1 BOTTLE, SPRAY (71753-8011-1) | 30 ml | 2020-09-30 | 2025-10-26 | No | No | Current |