MEDISON BELL PILL PATCH- tourmaline, magnesium sulfate, dimethyl sulfone, glucosamine kit

Medison Bell Pill Patch by

Drug Labeling and Warnings

Medison Bell Pill Patch by is a Otc medication manufactured, distributed, or labeled by SENNY STUDIO Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tourmaline, Magnesium sulfate, Dimethyl Sulfone, Glucosamine

PURPOSE

Effective for relieving muscle stiffness and joint pain.

INDICATIONS & USAGE

For external use only

WARNINGS

1. Do not use if you have skin conditions, eczema, or allergies.
2. If you experience swelling, pain, or red spots on the skin during use, stop using immediately and consult a physician.
3. Recommended use is up to 8 hours per day.
4. Store any unused patches in the resealable pouch to maintain effectiveness.
5. Keep out of reach of infants and children.
6. Do not use for purposes other than intended, and keep away from fire.
7. Avoid storing in temperatures above 30°C or in direct sunlight.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

1. Please clean the application area to remove any moisture or debris before use.
2. Peel the patch from the transparent film and place it on the desired area, pressing down firmly around the edges.

INACTIVE INGREDIENT

Mineral Oil, Hydrogenated polycyclopentadiene, Hydrogenated Styrene/Butadiene Copolymer, Menthol,

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDISON BELL PILL PATCH 
tourmaline, magnesium sulfate, dimethyl sulfone, glucosamine kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71829-0010

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71829-0010-1	1 in 1 CARTON	12/11/2024
1		1 in 1 POUCH; Type 0: Not a Combination Product

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	36 PATCH	36
Part 2	12 PATCH	12

Part 1 of 2

MEDISON BELL PILL PATCHTABLET 
tourmaline, magnesium sulfate, dimethyl sulfone, glucosamine liquid

Product Information
Item Code (Source)	NDC: 71829-0011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLUCOSAMINE (UNII: N08U5BOQ1K) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE	0.0045 g
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	0.0045 g
MAGNESIUM SULFATE (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM SULFATE	0.0135 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
MENTHOL (UNII: L7T10EIP3A)

Product Characteristics
Color		Score
Shape	ROUND (40x40mm)	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		1 in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other

Part 2 of 2

MEDISON BELL PILL PATCHCAPSULE 
tourmaline, magnesium sulfate, dimethyl sulfone, glucosamine liquid

Product Information
Item Code (Source)	NDC: 71829-0012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLUCOSAMINE (UNII: N08U5BOQ1K) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE	0.0155 g
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	0.0155 g
MAGNESIUM SULFATE (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM SULFATE	0.045 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
MENTHOL (UNII: L7T10EIP3A)

Product Characteristics
Color		Score
Shape	CAPSULE (122x85mm)	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		1 in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/11/2024

Labeler - SENNY STUDIO Co., Ltd (557827314)

Registrant - SENNY STUDIO Co., Ltd (557827314)

Establishment
Name	Address	ID/FEI	Business Operations
SENNY STUDIO Co., Ltd		557827314	manufacture(71829-0010)