Sun Pyrite 8X
NDC 48951-8433, Sun Pyrite 8X, powder, from Uriel Pharmacy, Inc.
- Product NDC
- 48951-8433
- Status
- Listed
- Labeler
- Uriel Pharmacy, Inc
- Dosage form
- POWDER
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/48951-8433 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FERROUS DISULFIDE8 [hp_X]/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 48951-8433-4 | 48951843304 | 50 g in 1 BOTTLE (48951-8433-4) |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 48951-8433 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/48951-8433 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 48951-8433. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.