Label: MSM2000 PREMIUM- methylsulfonylmethane tablet
-
Contains inactivated NDC Code(s)
NDC Code(s): 82437-020-01, 82437-020-02, 82437-020-03 - Packager: Vigen medical
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 15, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
-
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
- Uses
- Directions
- Other Information
- Questions
- PACKAGE LABEL82437-020-02 : 120 tablets
- PACKAGE LABEL82437-020-03 : 360 tablets
-
INGREDIENTS AND APPEARANCE
MSM2000 PREMIUM
methylsulfonylmethane tabletProduct 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)