MSM2000 PREMIUM- methylsulfonylmethane tablet

MSM2000 Premium by

Drug Labeling and Warnings

MSM2000 Premium by is a Otc medication manufactured, distributed, or labeled by Vigen medical, Pohangbiopark. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

METHYLSULFONYLMETHANE 99.0%

INACTIVE INGREDIENTS

Ascorbic acid fine powder (VitaminC), NLF01(Dextrin, Fermented Coconut Palm Oil, Cyclo Dextrin, Yam Extracted Powder, Red Ginseng Concentrate, Guarana Powder, Vitamin D3 Powder, Grapefruits Extracts

PURPOSE

To your healthy joints and cartilages

WARNINGS

■ Do not consume if there is anything wrong with product before ingestion.
■ If you have specific constitution or allergic, please check the ingredients before ingestion.
■ If a child swallows tablets, it can get caught in the throat, so care must be taken not to swallow them.
■ Infants, pregnant women, lactating women, disease holders, or those taking drugs should consult a doctor, pharmacist, etc. before ingestion.
■ Please be careful because you should not take the "dehumidifier" packaged separately for food quality control.
■ Consult with an expert in the case of an abnormal case.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

■ It can help to maintain joints and cartilages healthy

Directions

■ Take 2 tablets twice a day with sufficient water.

Other Information

■ When stored at high temperatures, tablets may melt and deform and deteriorate.
■ Keep it at room temperature to avoid moisture and direct sunlight, and avoid refrigeration.

Questions

■ Customer call
+82-1644-7582

PACKAGE LABEL82437-020-02 : 120 tablets

PACKAGE LABEL82437-020-03 : 360 tablets

INGREDIENTS AND APPEARANCE

MSM2000 PREMIUM 
methylsulfonylmethane tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82437-020
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	500 mg  in 506 mg

Inactive Ingredients
Ingredient Name	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R)

Product Characteristics
Color	white	Score	no score
Shape	OVAL	Size	14mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82437-020-02	120 in 1 CARTON	12/01/2021
1	NDC: 82437-020-01	506 mg in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 82437-020-03	360 in 1 CARTON	12/01/2021
2	NDC: 82437-020-01	506 mg in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2021

Labeler - Vigen medical (688763572)

Registrant - Vigen medical (688763572)

Establishment
Name	Address	ID/FEI	Business Operations
Pohangbiopark		688385519	manufacture(82437-020)