cuprum 0.4

Generic: cuprum 0.4

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

Drug Facts

Product Profile

Brand Name cuprum 0.4
Generic Name cuprum 0.4
Labeler uriel pharmacy, inc
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

copper 1 [hp_X]/g

Manufacturer
Uriel Pharmacy, Inc

Identifiers & Regulatory

Product NDC 48951-3280
Product ID 48951-3280_2c8fc7ec-a8ff-7468-e063-6294a90ae355
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Pharmacologic Class

Established (EPC)
copper-containing intrauterine device [epc]
Chemical Structure
copper [cs]
Physiologic Effect
decreased embryonic implantation [pe] decreased sperm motility [pe] inhibit ovum fertilization [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489513280
Hyphenated Format 48951-3280

Supplemental Identifiers

UNII
789U1901C5
NUI
M0005152 N0000175831 N0000008595 N0000008924 N0000175830

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 cuprum 0.4 (source: ndc)
Generic Name cuprum 0.4 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_X]/g
source: ndc
Packaging
  • 30 g in 1 TUBE (48951-3280-2)
source: ndc

Packages (1)

48951-3280-2 30 g in 1 TUBE (48951-3280-2)

Ingredients (1)

copper (1 [hp_X]/g)

Linked Drug Pages (1)

Cuprum 0.4 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c8fc7ec-a8ff-7468-e063-6294a90ae355", "openfda": {"nui": ["M0005152", "N0000175831", "N0000008595", "N0000008924", "N0000175830"], "unii": ["789U1901C5"], "spl_set_id": ["2c8fc7ec-a8fe-7468-e063-6294a90ae355"], "pharm_class_cs": ["Copper [CS]"], "pharm_class_pe": ["Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]"], "pharm_class_epc": ["Copper-containing Intrauterine Device [EPC]"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (48951-3280-2)", "package_ndc": "48951-3280-2", "marketing_start_date": "20090901"}], "brand_name": "Cuprum 0.4", "product_id": "48951-3280_2c8fc7ec-a8ff-7468-e063-6294a90ae355", "dosage_form": "OINTMENT", "pharm_class": ["Copper [CS]", "Copper-containing Intrauterine Device [EPC]", "Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]"], "product_ndc": "48951-3280", "generic_name": "Cuprum 0.4", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cuprum 0.4", "active_ingredients": [{"name": "COPPER", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}