Sun Pyrite 17X
- Product NDC
- 48951-8434
- 11-digit product format
- 489518434
- Labeler code
- 48951
- Product ID
- 48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sun Pyrite 17X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- FERROUS DISULFIDE
- Active strength
- 17 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 132N09W4PR | FERROUS DISULFIDE | 12068-85-8 | FERROUS DISULFIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8434-3 | 48951843403 | 60 mL in 1 BOTTLE, DROPPER (48951-8434-3) | 60 ml | 2009-09-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sun Pyrite 17X | Uriel Pharmacy, Inc | 2025-03-25 | HUMAN OTC DRUG LABEL | 1 |