United States · FDA National Drug Code directory

Helleborus comp. A

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 48951-5135_4420fb70-8e19-709c-e063-6394a90a1e7a
Product NDC: 48951-5135
Form: LIQUID
Composition / generic term: Helleborus comp. A
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20210311
Source listing expiry: 20261231

Source-listed ingredients

TIN — 12 [hp_X]/mL
PHOSPHORUS — 12 [hp_X]/mL
ARSENIC TRIOXIDE — 17 [hp_X]/mL
LEAD MONOSILICATE — 20 [hp_X]/mL
SILVER — 8 [hp_X]/mL
FORMICA RUFA — 6 [hp_X]/mL
ANTIMONY — 6 [hp_X]/mL
HELLEBORUS NIGER ROOT — 3 [hp_X]/mL
POTASSIUM PHOSPHATE, MONOBASIC — 6 [hp_X]/mL
JUGLANS REGIA LEAF — 7 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

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

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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