United States · FDA National Drug Code directory
Birch Juniper
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
- 48951-2149_43e13f9e-f46f-c5ad-e063-6394a90a25d7
- Product NDC
- 48951-2149
- Form
- LIQUID
- Composition / generic term
- Birch Juniper
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20211103
- Source listing expiry
- 20261231
Source-listed ingredients
- JUNIPER BERRY — 1 [hp_X]/mL
- BETULA PENDULA BARK — 1 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 240 mL in 1 BOTTLE, GLASS (48951-2149-9) · 48951-2149-9
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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