SupreH Bee Venom Arthritis Pain Relieving Cream

Manufacturer
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Effective date
2025-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:05:50

Label at a glance#

ProductSupreH Bee Venom Arthritis Pain Relieving Cream
Active ingredientARTEMISIA ARGYI WHOLE, APIS MELLIFERA VENOM, CARTHAMUS TINCTORIUS FLOWER BUD
Label structure13 sections

Dosage and administration

Adult s & children 12 years and over: Apply to affected areas no more than 3-4 times daily. Wash hands after applying. Children under 12 yrs: Ask a doctor.

Storage and handling

Store at room temperature, away from heat and direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Artemisia Argyi, Carthamus Tinctorius Flower Bud, Apis mellifera venom

Purpose

OTC - PURPOSE SECTION

Artemisia Argyi 1%……Topical analgesic
Carthamus Tinctorius Flower Bud 1.25%………Topical analgesic
Apis Mellifera Venom 1%……Topical analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief minor pain associated with arthritis, simple backache, muscle strains, sprains, bruises and joint stiffness

Warnings

WARNINGS SECTION

For external use only. Do not use this product on irritated skin, or on open wounds. Perform skin test prior to initial use.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Allergy Alert

OTHER SAFETY INFORMATION

Contains bee-derived ingredients. Do not use if you are allergic to bee stings.

When Using this product

OTC - WHEN USING SECTION

Avoid contact with eyes or mucous membranes.
Do not bandage tightly.

Stop use and ask a doctor if

OTC - STOP USE SECTION

1.Condition worsens
2.Pain persists more than 7 days
3.Rash or irritation develops

Directions

DOSAGE & ADMINISTRATION SECTION

Adult s & children 12 years and over:
Apply to affected areas no more than 3-4 times daily.
Wash hands after applying.

Children under 12 yrs:
Ask a doctor.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature, away from heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Commiphora Myrrha Resin, Eucommia Ulmoides Bark, Chinese Cinnamon, Zingiber Officinale Root, Boswellia Serrata Resin

Questions or comments?

OTC - QUESTIONS SECTION

Contact us at customerservice@supreh.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83818-016-01SupreH Bee Venom Arthritis Pain Relieving Cream100 g in 1 BOTTLECREAM1001

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
83818-01683818-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
SupreH Bee Venom Arthritis Pain Relieving CreamSUPREH BEE VENOM ARTHRITIS PAIN RELIEVING CREAMShenzhen Xinxin Yunhai Technology Co., Ltd.3876cc44-7f3a-b084-e063-6294a90a61422025-06-26WarningsExact identifier
ndc (package): 83818-016-01
ndc (product): 83818-016
ndc11 (package): 83818001601
spl id: 3876cc44-7f3b-b084-e063-6294a90a6142
spl set id: 3876cc44-7f3a-b084-e063-6294a90a6142

Reported adverse events (FAERS/openFDA)#

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