Vespa crabro 15X

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2024-11-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:29:02

Label at a glance#

ProductVespa crabro 15X

Active ingredientVESPA CRABRO

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Vespa crabro ex animale (Hornet) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of skin rash.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homepathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vespa crabro 15X Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-9385-1	Vespa crabro 15X	1 mL in 1 AMPULE	LIQUID	1		1
48951-9385-1	Vespa crabro 15X	10 in 1 BOX	LIQUID	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-9385	VESPA CRABRO 15X LIQUID [URIEL PHARMACY INC.]	1	2 package rows	20241123_278559af-be8d-cbd5-e063-6394a90a7a25.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Vespa crabro 15X
WATER
SODIUM CHLORIDE
VESPA CRABRO

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-9385	48951-9385-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
VESPA CRABRO	K3ALM8S49H	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
278559b9-4c7b-072a-e063-6394a90a00d2			278559af-be8d-cbd5-e063-6394a90a7a25	2024-11-22	Warnings	Exact identifier spl id: 278559b9-4c7b-072a-e063-6394a90a00d2 spl set id: 278559af-be8d-cbd5-e063-6394a90a7a25

Reported adverse events (FAERS/openFDA)#

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