helleborus comp. a

Generic: helleborus comp. a

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

Drug Facts

Product Profile

Brand Name helleborus comp. a
Generic Name helleborus comp. a
Labeler uriel pharmacy inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

antimony 6 [hp_X]/mL, arsenic trioxide 17 [hp_X]/mL, formica rufa 6 [hp_X]/mL, helleborus niger root 3 [hp_X]/mL, juglans regia leaf 7 [hp_X]/mL, lead monosilicate 20 [hp_X]/mL, phosphorus 12 [hp_X]/mL, potassium phosphate, monobasic 6 [hp_X]/mL, silver 8 [hp_X]/mL, tin 12 [hp_X]/mL

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-5135
Product ID 48951-5135_4420fb70-8e19-709c-e063-6394a90a1e7a
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2021-03-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489515135
Hyphenated Format 48951-5135

Supplemental Identifiers

UNII
9IT35J3UV3 S7V92P67HO 55H0W83JO5 608DGJ6815 85HKB87105 TLE92T7F1J 27YLU75U4W 4J9FJ0HL51 3M4G523W1G 387GMG9FH5

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 helleborus comp. a (source: ndc)
Generic Name helleborus comp. a (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 6 [hp_X]/mL
  • 17 [hp_X]/mL
  • 3 [hp_X]/mL
  • 7 [hp_X]/mL
  • 20 [hp_X]/mL
  • 12 [hp_X]/mL
  • 8 [hp_X]/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (48951-5135-1) / 1 mL in 1 AMPULE
source: ndc

Packages (1)

48951-5135-1 10 AMPULE in 1 BOX (48951-5135-1) / 1 mL in 1 AMPULE

Ingredients (10)

antimony (6 [hp_X]/mL) arsenic trioxide (17 [hp_X]/mL) formica rufa (6 [hp_X]/mL) helleborus niger root (3 [hp_X]/mL) juglans regia leaf (7 [hp_X]/mL) lead monosilicate (20 [hp_X]/mL) phosphorus (12 [hp_X]/mL) potassium phosphate, monobasic (6 [hp_X]/mL) silver (8 [hp_X]/mL) tin (12 [hp_X]/mL)

Linked Drug Pages (1)

Helleborus comp. A ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4420fb70-8e19-709c-e063-6394a90a1e7a", "openfda": {"unii": ["9IT35J3UV3", "S7V92P67HO", "55H0W83JO5", "608DGJ6815", "85HKB87105", "TLE92T7F1J", "27YLU75U4W", "4J9FJ0HL51", "3M4G523W1G", "387GMG9FH5"], "spl_set_id": ["150e57ad-3ed7-5cc9-e063-6394a90a25fe"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-5135-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-5135-1", "marketing_start_date": "20210311"}], "brand_name": "Helleborus comp. A", "product_id": "48951-5135_4420fb70-8e19-709c-e063-6394a90a1e7a", "dosage_form": "LIQUID", "product_ndc": "48951-5135", "generic_name": "Helleborus comp. A", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Helleborus comp. A", "active_ingredients": [{"name": "ANTIMONY", "strength": "6 [hp_X]/mL"}, {"name": "ARSENIC TRIOXIDE", "strength": "17 [hp_X]/mL"}, {"name": "FORMICA RUFA", "strength": "6 [hp_X]/mL"}, {"name": "HELLEBORUS NIGER ROOT", "strength": "3 [hp_X]/mL"}, {"name": "JUGLANS REGIA LEAF", "strength": "7 [hp_X]/mL"}, {"name": "LEAD MONOSILICATE", "strength": "20 [hp_X]/mL"}, {"name": "PHOSPHORUS", "strength": "12 [hp_X]/mL"}, {"name": "POTASSIUM PHOSPHATE, MONOBASIC", "strength": "6 [hp_X]/mL"}, {"name": "SILVER", "strength": "8 [hp_X]/mL"}, {"name": "TIN", "strength": "12 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20210311", "listing_expiration_date": "20261231"}