OTC - ACTIVE INGREDIENT SECTION
Bee Venom Extract：7.5 mg in 30 g
Arnica Chamissonis Flower Extract：4.5 mg in 30 g
Glucosamine：4.5 mg in 30 g
Menaquinone-7：4.5 mg in 30 g
Dimethyl Sulfone：4.5 mg in 30 g
Bee Venmo Pain Cream
- Manufacturer
- Shenzhenshishengyakeji Co., Ltd.
- Effective date
- 2024-10-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:51:05
Label at a glance#
ProductBee Venmo Pain Cream
Active ingredientDIMETHYL SULFONE, MENAQUINONE-7, ARNICA CHAMISSONIS FLOWER EXTRACT, GLUCOSAMINE
Label structure10 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
soothe joints swelling,and reduce pain and discomfort.
OTC - ASK DOCTOR SECTION
Conditon worse or doesnot improve after regular use as directed
DOSAGE & ADMINISTRATION SECTION
1.Clean and dry the affected area of skin.
2.Take an appropriate amount of cream and apply lt eyenly on the skin.
3.Massage gently with your hands in circular motions for absorption.
4.Use it 2-3 times a day for batter results.
OTC - WHEN USING SECTION
Please clean your hands before use to ensure the best results from the product.
WARNINGS SECTION
Please keep out of reach of chldren.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry niace.
INDICATIONS & USAGE SECTION
soothe joints swelling,and reduce pain and discomfort.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Please keep out of reach of children.
INACTIVE INGREDIENT SECTION
Sodium Butyroyl/Formoyl Chondroitin Sulfate:4.5 mg in 30 g
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Bee Venmo Pain Cream
- DIMETHYL SULFONE
- SODIUM BUTYROYL/FORMOYL HYALURONATE
- MENAQUINONE-7
- ARNICA CHAMISSONIS FLOWER EXTRACT
- GLUCOSAMINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84752-016 | 84752-016-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIMETHYL SULFONE | 9H4PO4Z4FT | ACTIB |
| SODIUM BUTYROYL/FORMOYL HYALURONATE | F63GOY24UQ | IACT |
| MENAQUINONE-7 | 8427BML8NY | ACTIB |
| ARNICA CHAMISSONIS FLOWER EXTRACT | 88WK5I8R3L | ACTIB |
| GLUCOSAMINE | N08U5BOQ1K | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 256f4182-ace4-c6d2-e063-6394a90a4807 | 256f4182-ace3-c6d2-e063-6394a90a4807 | 2024-10-27 | Warnings | 256f4182-ace4-c6d2-e063-6394a90a4807 256f4182-ace3-c6d2-e063-6394a90a4807 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.