FDA.reportPublic FDA data

YELLOW WAX

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:29:30

Label at a glance#

ProductEucalyptus comp.
Active ingredientDROSERA ROTUNDIFOLIA, PETASITES HYBRIDUS ROOT, PLANTAGO MAJOR LEAF
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Drosera (Sundew) 1X, Petasites (Butterbur) 1X, Plantago (Ribwort plantain) 1X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Beeswax, Lanolin, Spring water, Larch resin, Sunflower seed oil, Distilled water, Eucalyptus oil, Lavender oil, Thyme oil, Sorbic acid, Tea tree oil, Grapefruit seed extract

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of flu symptoms.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: FOR EXTERNAL USE ONLY.
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

Eucalyptus comp. OintmentEucalyptus comp. 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
48951-4194-5Eucalyptus comp.60 g in 1 TUBEOINTMENT601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4194EUCALYPTUS COMP. OINTMENT [URIEL PHARMACY INC.]11 package rows20241213_29010ef0-4da4-ebe7-e063-6294a90a7380.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-419448951-4194-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
YELLOW WAX2ZA36H0S2VIACT
LANOLIN7EV65EAW6HIACT
WATER059QF0KO0RIACT
LARIX DECIDUA RESINAD8LJ73GQFIACT
SUNFLOWER OIL3W1JG795YIIACT
EUCALYPTUS OIL2R04ONI662IACT
LAVENDER OILZBP1YXW0H8IACT
THYME OIL2UK410MY6BIACT
SORBIC ACIDX045WJ989BIACT
CITRUS PARADISI SEED12F08874Y7IACT
DROSERA ROTUNDIFOLIAQR44N9XPJQACTIB
PETASITES HYBRIDUS ROOT97S2809V5RACTIB
OLIVE OIL6UYK2W1W1EIACT
PLANTAGO MAJOR LEAF7DC28K241XACTIB
TEA TREE OILVIF565UC2GIACT

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
29010efb-0f2f-6296-e063-6294a90a443e29010ef0-4da4-ebe7-e063-6294a90a73802024-12-11WarningsExact identifier
spl id: 29010efb-0f2f-6296-e063-6294a90a443e
spl set id: 29010ef0-4da4-ebe7-e063-6294a90a7380

Reported adverse events (FAERS/openFDA)#

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