sun pyrite 17x

Generic: sun pyrite 17x

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

Drug Facts

Product Profile

Brand Name sun pyrite 17x
Generic Name sun pyrite 17x
Labeler uriel pharmacy, inc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

ferrous disulfide 17 [hp_X]/mL

Manufacturer
Uriel Pharmacy, Inc

Identifiers & Regulatory

Product NDC 48951-8434
Product ID 48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708
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 489518434
Hyphenated Format 48951-8434

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 17x (source: ndc)
Generic Name sun pyrite 17x (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 17 [hp_X]/mL
source: ndc
Packaging
  • 60 mL in 1 BOTTLE, DROPPER (48951-8434-3)
source: ndc

Packages (1)

48951-8434-3 60 mL in 1 BOTTLE, DROPPER (48951-8434-3)

Ingredients (1)

ferrous disulfide (17 [hp_X]/mL)

Linked Drug Pages (1)

Sun Pyrite 17X ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3130d5c4-fa48-f6af-e063-6294a90a3708", "openfda": {"unii": ["132N09W4PR"], "spl_set_id": ["3130d5c4-fa47-f6af-e063-6294a90a3708"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, DROPPER (48951-8434-3)", "package_ndc": "48951-8434-3", "marketing_start_date": "20090901"}], "brand_name": "Sun Pyrite 17X", "product_id": "48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708", "dosage_form": "LIQUID", "product_ndc": "48951-8434", "generic_name": "Sun Pyrite 17X", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sun Pyrite 17X", "active_ingredients": [{"name": "FERROUS DISULFIDE", "strength": "17 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}