Natralia Eczema and Psoriasis
- Product NDC
- 43251-2281
- 11-digit product format
- 432512281
- Labeler code
- 43251
- Product ID
- 43251-2281_e8fe71f0-8778-410f-b5f7-3c8e4cf9567b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Borate, Graphite, Potassium Sulfate, and Sodium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- LaCorium Health USA Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-01-03
- Marketing end
- 2022-08-31
- Substance
- SODIUM BORATE; GRAPHITE; POTASSIUM SULFATE; SODIUM CHLORIDE
- Active strength
- 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43251-2281-1 | 43251228101 | 200 mL in 1 BOTTLE (43251-2281-1) | 200 ml | 2009-01-03 | 2022-08-31 | No | No | Current |