FDA.reportPublic FDA data

Bee Venom Nail Serum

Manufacturer
Dongguan Haiyi Cosmetics Co., Ltd.
Effective date
2025-08-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:09:55

Label at a glance#

ProductBee Venom Nail Serum
Active ingredientAPIS MELLIFERA VENOM
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

APIS MELLIFERA VENOM

INACTIVE INGREDIENT SECTION

Aqua, PrunusAmygdalus Dulcis (SweetAlmond) Oil, LinumUsitatissimum (Linseed) Seed Oil,Melaleuca Alternifolia (Tea Tree)Leaf Oil, Tocopherol, HydrolyzedKeratin

OTC - PURPOSE SECTION

Eliminate Fungal infections

Cuticle Care

Prevent Infections

Nail Strengthening& sharpening

WARNINGS SECTION

1).For external use only, avoid directcontact with eyes, lf you feel any
discomfort, stop using itand wash it with plenty of water. In severe cases,
pleaseseek medical attention in time.
2). Not allowed to be used ondamaged skin,

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

INDICATIONS & USAGE SECTION

1. First clean the affected nailcompletely and dry it.

2. Take an appropriate amount ofthis product and apply it evenly on the nails.

3. Wait 2-3 minutes for full absorption.

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85594-008-15Bee Venom Nail Serum15 mL in 1 BOTTLELIQUID151

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
85594-00885594-008-15

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
AQUA059QF0KO0RIACT
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL66YXD4DKO9IACT
TOCOPHEROLR0ZB2556P8IACT
COCODIMONIUM HYDROXYPROPYL HYDROLYZED KERATIN (1000 MW)8V0I3U3HMOIACT
LINUM USITATISSIMUM (LINSEED) SEED OIL84XB4DV00WIACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
APIS MELLIFERA VENOM76013O881MACTIB

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
3c1348d3-286f-1672-e063-6294a90a34e33c1348d3-286e-1672-e063-6294a90a34e32025-08-11WarningsExact identifier
spl id: 3c1348d3-286f-1672-e063-6294a90a34e3
spl set id: 3c1348d3-286e-1672-e063-6294a90a34e3

Reported adverse events (FAERS/openFDA)#

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