United States · FDA National Drug Code directory
Plantain Beeswax
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
- 48951-8419_2b247033-d7c4-61c6-e063-6394a90a48f6
- Product NDC
- 48951-8419
- Form
- OINTMENT
- Composition / generic term
- Plantain Beeswax
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20090901
- Source listing expiry
- 20261231
Source-listed ingredients
- PETASITES HYBRIDUS ROOT — 4 [hp_X]/g
- LARIX DECIDUA RESIN — 1 [hp_X]/g
- SAGE — 3 [hp_X]/g
- DROSERA ROTUNDIFOLIA — 4 [hp_X]/g
- PLANTAGO MAJOR LEAF — 4 [hp_X]/g
These values do not establish equivalence or a dose recommendation.
Packages
- 60 g in 1 TUBE (48951-8419-5) · 48951-8419-5
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 →