FDA.reportPublic FDA data

Vespa crabro

Manufacturer
Uriel Pharmacy Inc.
Effective date
2026-08-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-08-18 02:01:40

Label at a glance#

ProductVespa Crabro DKS
Active ingredientVISCUM ALBUM FRUITING TOP, ROYAL JELLY, ANTIMONY, COPPER, URTICA DIOICA, SEDUM ROSEUM WHOLE, GOLD, BOS TAURUS PLACENTA, TIN, VESPA CRABRO
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: Apis regina (Queen Bee cell with larva and nutrient fluid) 6X/15X, Stannum met. (Metallic tin) 6X/15X, Stibium met. (Antimony) 6X/15X,Vespa crabro (Hornet) 6X/16X/30X, Cinis Urtica dioicae (Stinging nettle ash) 8X, Viscum Mali (Apple tree mistletoe) 8X/15X, Rosa (Garden rose) 10X, Aurum met. (Metallic gold) 10X/15X, Placenta bovis (Bovine placenta) 8X, Cuprum met. (Copper) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Lanolin, Beeswax, Lanolin alcohol, Grapefruit seed extract, Lactose

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 homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains traces of lactose. 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: Rev.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vespa crabro OintmentVespa crabro Ointment

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-9370-52026-01-29C16284748780-149896155-a950-586f-e063-e6dba90add90Vespa crabro DKS
48951-9370-52026-01-29C16284748780-149896155-a950-586f-e063-e6dba90add90Vespa crabro

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-939648951-9396-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
VISCUM ALBUM FRUITING TOPBK9092J5MPACTIB
ROYAL JELLYL497I37F0CACTIB
ANTIMONY9IT35J3UV3ACTIB
COPPER789U1901C5ACTIB
URTICA DIOICA710FLW4U46ACTIB
SEDUM ROSEUM WHOLERH0WP583U3ACTIB
GOLD79Y1949PYOACTIB
BOS TAURUS PLACENTA83AL37E3A7ACTIB
TIN387GMG9FH5ACTIB
VESPA CRABROK3ALM8S49HACTIB
LANOLIN ALCOHOLS884C3FA9HEIACT
OLIVE OIL6UYK2W1W1EIACT
LANOLIN7EV65EAW6HIACT
YELLOW WAX2ZA36H0S2VIACT
CITRUS PARADISI SEED12F08874Y7IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-15full-release2026-06-01 02:28:54

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
Vespa Crabro DKSVESPA CRABRO DKSUriel Pharmacy Inc.06e9e1ff-911f-c048-e063-6394a90ad4312026-08-14WarningsExact identifier
ndc (package): 48951-9396-5
ndc (product): 48951-9396
ndc11 (package): 48951939605
spl id: 59048b19-1838-8726-e063-6294a90af135
spl set id: 06e9e1ff-911f-c048-e063-6394a90ad431

Reported adverse events (FAERS/openFDA)#

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