sun pyrite 8x

Generic: sun pyrite 8x

Labeler: uriel pharmacy, inc
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name sun pyrite 8x
Generic Name sun pyrite 8x
Labeler uriel pharmacy, inc
Dosage Form POWDER
Routes
ORAL
Active Ingredients

ferrous disulfide 8 [hp_X]/g

Manufacturer
Uriel Pharmacy, Inc

Identifiers & Regulatory

Product NDC 48951-8433
Product ID 48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489518433
Hyphenated Format 48951-8433

Supplemental Identifiers

UNII
132N09W4PR

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sun pyrite 8x (source: ndc)
Generic Name sun pyrite 8x (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 [hp_X]/g
source: ndc
Packaging
  • 50 g in 1 BOTTLE (48951-8433-4)
source: ndc

Packages (1)

48951-8433-4 50 g in 1 BOTTLE (48951-8433-4)

Ingredients (1)

ferrous disulfide (8 [hp_X]/g)

Linked Drug Pages (1)

Sun Pyrite 8X ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2eae3f2d-b712-0f50-e063-6294a90a8349", "openfda": {"unii": ["132N09W4PR"], "spl_set_id": ["2eae3f2d-b711-0f50-e063-6294a90a8349"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (48951-8433-4)", "package_ndc": "48951-8433-4", "marketing_start_date": "20090901"}], "brand_name": "Sun Pyrite 8X", "product_id": "48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349", "dosage_form": "POWDER", "product_ndc": "48951-8433", "generic_name": "Sun Pyrite 8X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sun Pyrite 8X", "active_ingredients": [{"name": "FERROUS DISULFIDE", "strength": "8 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}