FDA.reportPublic FDA data

SOUTH MOON Melittin Joint Soothing Gel

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:27:40

Label at a glance#

ProductSOUTH MOON Melittin Joint Soothing Gel
Active ingredientAPIS MELLIFERA VENOM, GLUCOSAMINE
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BEE VENOM

GLUCOSAMINE

Inactive ingredient

INACTIVE INGREDIENT SECTION

AQUA,CURCUMIN,EICOSAPENTAENOIC ACID,CHOLE-CALCIFEROL

Purpose section

OTC - PURPOSE SECTION

1.Solve various joint problems

2.passed the USA FDAapproved

3.Effectively relieves arthritis pain

4.Does not contain anyharmful ingredients.

Warning

WARNINGS SECTION

Please keep out of reachof children. Do notswallow.Please clean yourhands before use to ensurethe best results from theproduct. Discontinue useif signs of irritation or rashoccur. Store in a cool and dry place.

stop use

OTC - STOP USE SECTION

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

not use

OTC - DO NOT USE SECTION

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

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

1. Clean and dry the skin onthe joints.

2. Take an appropriateamount of gel and apply itevenly on the joints.

3. Gently massage withhands in circular motionuntil absorbed.

4. Daily use can get betterresults.

Dosage

DOSAGE & ADMINISTRATION SECTION

take an appropriateamount,Use 2-3 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f6766515-27b8-72de-2010-167151236aceProduct name720251021
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-055-012025-07-29C16284748780-13b156c62-2c4d-fb37-e063-e6dba90a4e0724f5078b-317c-ddf6-e063-6394a90a64cf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-055-01SOUTH MOON Melittin Joint Soothing Gel20 g in 1 TUBEGEL201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-055SOUTH MOON MELITTIN JOINT SOOTHING GEL GEL [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241022_24f5078b-317c-ddf6-e063-6394a90a64cf.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-05584732-055-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA VENOM76013O881MACTIB
WATER059QF0KO0RIACT
CURCUMINIT942ZTH98IACT
GLUCOSAMINEN08U5BOQ1KACTIB
CHOLECALCIFEROL1C6V77QF41IACT
ICOSAPENTAAN7QOV9EAIACT

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
24f5078b-317d-ddf6-e063-6394a90a64cf24f5078b-317c-ddf6-e063-6394a90a64cf2024-10-20WarningsExact identifier
spl id: 24f5078b-317d-ddf6-e063-6394a90a64cf
spl set id: 24f5078b-317c-ddf6-e063-6394a90a64cf

Reported adverse events (FAERS/openFDA)#

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