FDA.reportPublic FDA data

BEEVENOM

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2012-09-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:45:50

Label at a glance#

ProductBEEVENOM
Active ingredientGlycerin, Dimethicone
Label structure8 sections

Indications and uses

How to Use: At the last step of your skin care, apply an appropriate amount over face and neck.

Dosage and administration

How to Use: At the last step of your skin care, apply an appropriate amount over face and neck.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Glycerin 20%, Dimethicone 1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Butylene Glycol, Cyclopentasiloxane, Dimethiconol, Alcohol Denat., Polysilicone-11, Phenyl Trimethicone, Ethylhexyl Palmitate, Pentylene Glycol, Phenoxyethanol, Bee Venom, Ammonium Acryloyldimethyltaurate/VP Copolymer, Carbomer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Tromethamine, Olea Europaea (Olive) Fruit Oil, Lavandula Angustifolia (Lavender) Oil, Pinus Sylvestris Leaf Oil, Cananga Odorata Flower Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Pelargonium Graveolens Flower Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Camellia Japonica Flower Extract, Dipotassium Glycyrrhizate, Phospholipids, Silver, Polydecene, Squalane, Viscum Album (Mistletoe) Fruit Extract, Salicylic Acid, Ascorbic Acid

PURPOSE

OTC - PURPOSE SECTION

Purpose: Formulated with 69% bee venom complex, this cream is for skin that gets easily irritated and suffers from redness.

WARNINGS

WARNINGS SECTION

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

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

How to Use: At the last step of your skin care, apply an appropriate amount over face and neck.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

How to Use: At the last step of your skin care, apply an appropriate amount over face and neck.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809344261175GTIN-13: 8809344261175
EAN-13: 8809344261175
GTIN storage (14 digits): 08809344261175		beevenom carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-110-012021-07-05C16284748780-19d75b9d0-df39-f424-e053-dadaa90a57ceee350f2b-5f5d-4a43-adb5-82a069d4befb
51346-110-012020-01-31C16284748780-19d75b9d0-df39-f424-e053-dadaa90a57ceee350f2b-5f5d-4a43-adb5-82a069d4befb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DimethiconeACTIVE INGREDIENT92RU3N3Y1O1
GlycerinACTIVE INGREDIENTPDC6A3C0OX1
DimethiconeACTIVE MOIETY92RU3N3Y1O1
GlycerinACTIVE MOIETYPDC6A3C0OX1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
Ethylhexyl PalmitateINACTIVE INGREDIENT28659933091
Pentylene GlycolINACTIVE INGREDIENT50C1307PZG1
Phenyl TrimethiconeINACTIVE INGREDIENTDR0K5NOJ4R1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-11051346-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GlycerinPDC6A3C0OXACTIM
Dimethicone92RU3N3Y1OACTIM
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT
Phenyl TrimethiconeDR0K5NOJ4RIACT
Ethylhexyl Palmitate2865993309IACT
Pentylene Glycol50C1307PZGIACT

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
35e13cc1-ef67-4c45-9dcc-995d3e5db92dee350f2b-5f5d-4a43-adb5-82a069d4befb2021-07-02WarningsExact identifier
spl set id: ee350f2b-5f5d-4a43-adb5-82a069d4befb

Reported adverse events (FAERS/openFDA)#

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