Natrum Phosphoricum
- Product NDC
- 71753-8010
- 11-digit product format
- 717538010
- Labeler code
- 71753
- Product ID
- 71753-8010_f8f8d698-66d8-409e-a9f9-38118cb3fc7a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Natrum Phosphoricum
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Ratis, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-09-30
- Marketing end
- 2025-10-26
- Substance
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
- 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 |
|---|
| 71753-8010 | NATRUM PHOSPHORICUM SPRAY [RATIS, LLC] | 2 | Legacy NDC | 20220121_3b808bfc-551a-4561-ab11-2f91e030aef7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71753-8010-1 | 71753801001 | 30 mL in 1 BOTTLE, SPRAY (71753-8010-1) | 30 ml | 2020-09-30 | 0000-00-00 | No | No | Current |