United States · FDA National Drug Code directory

Cartilago Betula

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
48951-3039_4484e015-d695-b864-e063-6394a90aa9a3
Product NDC
48951-3039
Form
LIQUID
Composition / generic term
Cartilago Betula
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20090901
Source listing expiry
20261231

Source-listed ingredients

  • BETULA PUBESCENS LEAF — 5 [hp_X]/mL
  • ACONITUM NAPELLUS — 6 [hp_X]/mL
  • ARNICA MONTANA — 6 [hp_X]/mL
  • BOS TAURUS CARTILAGE — 8 [hp_X]/mL
  • TIN — 8 [hp_X]/mL
  • GOLD — 10 [hp_X]/mL
  • ONION — 17 [hp_X]/mL
  • FORMICA RUFA — 17 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 AMPULE in 1 BOX (48951-3039-1) / 1 mL in 1 AMPULE · 48951-3039-1

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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