BEE VENOM TREATMENT SPOT

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-11-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:10:02

Label at a glance#

ProductBEE VENOM TREATMENT SPOT
Active ingredientGLYCERIN
Label structure8 sections

Dosage and administration

Directions 1. Apply an appropriate amount to the problem areas 2. Gently rub to enhance absorption into skin

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: GLYCERIN (4.05%)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:

Water, Butylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Simmondsia Chinensis (Jojoba) Seed Oil, 1,2-Hexanediol, Sodium Polyacrylate, Polyglyceryl-3 Methylglucose Distearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glyceryl Stearate, Peg-100 Stearate, Phenoxyethanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Arginine, Xylitol, Olea Europaea (Olive) Fruit Oil, Disodium Edta, Beta-Sitosterol, Alcohol Denat., Centella Asiatica Extract, Steareth-4, Cholesterol, Potassium Cetyl Phosphate, Propylene Glycol, Salicylic Acid, Tocopherol, Lavandula Angustifolia (Lavender) Oil, Pinus Sylvestris Leaf Oil, Cananga Odorata Flower Oil, Pollen Extract, Macadamia Ternifolia Seed Oil, Cholesteryl/Behenyl/Octyldodecyl Lauroyl Glutamate, Palmeth-2 Phosphate, Rosmarinus Officinalis (Rosemary) Leaf Oil, Origanum Vulgare Leaf Extract, Salix Alba (Willow) Bark Extract, Chamaecyparis Obtusa Leaf Extract, Pelargonium Graveolens Flower Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Camellia Japonica Flower Extract, Portulaca Oleracea Extract, Scutellaria Baicalensis Root Extract, Lactobacillus/Soybean Ferment Extract, Cinnamomum Cassia Bark Extract, Water, Terminalia Chebula Fruit Extract, Caesalpinia Sappan Bark Extract, Magnolia Obovata Bark Extract, Alcohol, Bee Venom, Lecithin

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Skin Protectant

WARNINGS

WARNINGS SECTION

WARNINGS:

For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage:

Concentrated spot care ointment for acne.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

1. Apply an appropriate amount to the problem areas 2. Gently rub to enhance absorption into skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138806173425914GTIN-13: 8806173425914
EAN-13: 8806173425914
GTIN storage (14 digits): 08806173425914
spot carton.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-36551346-365-01

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
NameUNIIKind
GLYCERINPDC6A3C0OXACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
62772968-278d-4955-9182-3d372cbb5df755e07fbf-7dec-452d-a3aa-765e53575c862017-11-20WarningsExact identifier
spl id: 62772968-278d-4955-9182-3d372cbb5df7
spl set id: 55e07fbf-7dec-452d-a3aa-765e53575c86

Reported adverse events (FAERS/openFDA)#

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