United States · FDA National Drug Code directory
Betula Argentum
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
- 48951-2063_3894ea71-3636-1458-e063-6394a90a08fd
- Product NDC
- 48951-2063
- Form
- LIQUID
- Composition / generic term
- Betula Argentum
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20090901
- Source listing expiry
- 20261231
Source-listed ingredients
- APIS MELLIFERA — 3 [hp_X]/mL
- BETULA PUBESCENS BARK — 3 [hp_X]/mL
- BETULA PUBESCENS LEAF — 3 [hp_X]/mL
- FORMICA RUFA — 7 [hp_X]/mL
- SILVER — 8 [hp_X]/mL
- ARNICA MONTANA — 17 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 AMPULE in 1 BOX (48951-2063-1) / 1 mL in 1 AMPULE · 48951-2063-1
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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