Sun Pyrite 8X
- Product NDC
- 48951-8433
- 11-digit product format
- 489518433
- Labeler code
- 48951
- Product ID
- 48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sun Pyrite 8X
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- FERROUS DISULFIDE
- Active strength
- 8 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sun Pyrite 8X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FERROUS DISULFIDE | 8 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 132N09W4PR |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8433-4 | Sun Pyrite 8X | 50 g in 1 BOTTLE | POWDER | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8433 | SUN PYRITE 8X POWDER [URIEL PHARMACY, INC] | 1 | Current NDC, 1 package rows | 20250309_2eae3f2d-b711-0f50-e063-6294a90a8349.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8433-4 | 48951843304 | 50 g in 1 BOTTLE (48951-8433-4) | 50 g | 2009-09-01 | No | No | Current |