Vespa Crabro DKS

Manufacturer
Uriel Pharmacy Inc.
Effective date
2021-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:44:05

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) 11X, Cuprum met. (Copper) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic olive oil, Lanolin, Beeswax, Lanolin alcohol, Grapefruitseed extract, Sorbic acid, Lactose

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: 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. Contains traces of lactose. 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
www.urielpharmacy.com Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vespa Crabro DKS OintmentVespa Crabro DKS Ointment

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-936548951-9365-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

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
06fa49fb-03c5-ac7a-e063-6394a90aea07c3ce914a-ab38-641a-e053-2a95a90a54fd2023-10-03WarningsExact identifier
spl set id: c3ce914a-ab38-641a-e053-2a95a90a54fd

Reported adverse events (FAERS/openFDA)#

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