Home NDC 48951-8419 Plantain Beeswax
Product NDC 48951-8419
11-digit product format 489518419
Labeler code 48951
Product ID 48951-8419_2b247033-d7c4-61c6-e063-6394a90a48f6
Type HUMAN OTC DRUG
Nonproprietary name Plantain Beeswax
Dosage form OINTMENT
Route TOPICAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance DROSERA ROTUNDIFOLIA; LARIX DECIDUA RESIN; PETASITES HYBRIDUS ROOT; PLANTAGO MAJOR LEAF; SAGE
Active strength 4; 1; 4; 4; 3 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Plantain Beeswax
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength 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
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8419-5 Plantain Beeswax 60 g in 1 TUBE OINTMENT 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8419 PLANTAIN BEESWAX OINTMENT [URIEL PHARMACY INC.] 2 Current NDC, 1 package rows 20250109_26facd12-ab50-e2c4-e063-6394a90ae8d1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 48951-8419-5 48951841905 60 g in 1 TUBE (48951-8419-5) 60 g 2009-09-01 No No Current