FDA.reportPublic FDA data

Plantain Beeswax

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:30:06

Label at a glance#

ProductPlantain Beeswax
Active ingredientPETASITES HYBRIDUS ROOT, LARIX DECIDUA RESIN, SAGE, DROSERA ROTUNDIFOLIA, PLANTAGO MAJOR LEAF
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to the chest, back and soles of feet in the morning and evening or as needed, and cover warmly. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 100 gm contains: 50 gm Resina laricis (Larch resin) 1X; Salvia e fol. (Sage) 3X, Drosera ex herba (Sundew) 4X, Petasites e rad. (Butterbur) 4X, Plantago e fol. (Plantain) 4X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Beeswax, Lanolin, Spring water, Camphor, Glycerin, Eucalyptus oil, Lavender oil, Thyme oil, Sodium alginate, Sage oil, Tea tree, Grapefruit seed extract

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Uses: Temporary relief of cough and chest congestion.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Plantain Beeswax OintmentPlantain Beeswax Ointment

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8419-5Plantain Beeswax60 g in 1 TUBEOINTMENT602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8419PLANTAIN BEESWAX OINTMENT [URIEL PHARMACY INC.]2Current NDC, 1 package rows20250109_26facd12-ab50-e2c4-e063-6394a90ae8d1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-841948951-8419-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
PETASITES HYBRIDUS ROOT97S2809V5RACTIB
OLIVE OIL6UYK2W1W1EIACT
YELLOW WAX2ZA36H0S2VIACT
LANOLIN7EV65EAW6HIACT
WATER059QF0KO0RIACT
CAMPHOR (NATURAL)N20HL7Q941IACT
GLYCERINPDC6A3C0OXIACT
EUCALYPTUS OIL2R04ONI662IACT
LAVENDER OILZBP1YXW0H8IACT
THYME OIL2UK410MY6BIACT
SODIUM ALGINATEC269C4G2ZQIACT
TEA TREE OILVIF565UC2GIACT
SAGE OILU27K0H1H2OIACT
CITRUS PARADISI SEED12F08874Y7IACT
LARIX DECIDUA RESINAD8LJ73GQFACTIB
SAGE065C5D077JACTIB
DROSERA ROTUNDIFOLIAQR44N9XPJQACTIB
PLANTAGO MAJOR LEAF7DC28K241XACTIB

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Plantain BeeswaxPLANTAIN BEESWAXUriel Pharmacy Inc.26facd12-ab50-e2c4-e063-6394a90ae8d12025-01-07WarningsExact identifier
ndc (package): 48951-8419-5
ndc (product): 48951-8419
ndc11 (package): 48951841905
spl id: 2b247033-d7c4-61c6-e063-6394a90a48f6
spl set id: 26facd12-ab50-e2c4-e063-6394a90ae8d1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.