United States · FDA National Drug Code directory

Sabal Populus

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
48951-8161_5387cb83-9b53-aa07-e063-6394a90ac899
Product NDC
48951-8161
Form
LIQUID
Composition / generic term
Sabal Populus
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20090901
Source listing expiry
20271231

Source-listed ingredients

  • BERBERIS VULGARIS ROOT BARK — 3 [hp_X]/mL
  • POPULUS TREMULA WHOLE — 3 [hp_X]/mL
  • SAW PALMETTO — 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP — 3 [hp_X]/mL
  • THUJA OCCIDENTALIS WHOLE — 6 [hp_X]/mL
  • MAGNESITE — 12 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 AMPULE in 1 BOX (48951-8161-1) / 1 mL in 1 AMPULE · 48951-8161-1

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →