Label: SEA MOSS DIETARY SUPPLEMENT capsule

  • NDC Code(s): 83872-996-01
  • Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT SECTION

    Vitamin C (as Ascorbic Acid)90 mg 100%
    Vitamin D3 (as Cholecalciferol) (2000 IU)25 mcg 125%
    Sea Moss (Chondrus crispus 20:1 Extract) (Whole Plant)(Equivalent to 7000mg of raw Sea Moss powder)350mg
    Black Seed (Nigella Sativa 20:1Extract)(Equivalent to 4000mg of raw Black Seed Oil Powder)200mg
    Ashwagandha (Withania Somnifera 20:1Extract)(Equivalent to 2000mg of raw Ashwagandha powder)100mg
    Turmeric (Curcuma Longa 20:1 Extract) (Root)(Equivalent to 2000mg of raw Tumeric Powder)100mg
    Bladderwrack (Fucus Vesiculosus 20:1Extract) (Whole Plant)(Equivalent to 2000mg of raw Bladderwrack Powder)100mg
    Burdock (Arctium 20:1 Extract)(Root)(Equivalent to 2000mg of raw Burdock Powder)100mg
    Multimineral Blend
    Apple Cider Vinegar (Malus domestica) (Fruit) Powder, Dandelion (Taraxao11officinale) (Root) Extract, Yellow Dock (Rumex crispus) (Root) Powder, Eld(Sambucus willamsii hance) (Fruit) Extract, Manuka Honey (Leptospermum scoparium)(Root) Powder, Ginger (Zingiber officinale), Chlorophyll.350mgBlack Pepper (Piper nigrum)(Fruit) Extract5 mg

  • PURPOSE


    Supplements are used to supplement nutrients that are insufficient in dietary intake;
    Health products are for consumption by specific groups of people and have the function of regulating specific body functions;
    Medicines are used to prevent, treat and diagnose diseases in humans.

  • Uses

    If used with other medicines as directed (see Instructions for Use)

    Children need to use it under adult supervision.

  • Warnings


    Do not take supplements in place of or with prescription medications without your healthcare provider's approval. Need surgery
    Surgery, please check with your healthcare provider about the supplements you take.

  • CAUTION


    Do not exceed recommended dose,Pregnant or nursing mothers,children derthe age of 18,and individuals with a knownmedical condition should consult a physicianbefore using this or any dietary supplement.

  • When using this product


    Take one (1) capsule daily, or as directed by your health care professional.

  • Stop use and ask a doctor

    If you experience allergic or other adverse reactions after taking it, please stop using it immediately.

  • KEEP OUT OF THE REACH OF CHILDREN.


    Keep out of the reach of children. Do not use if safety seal is damaged or missing, store in a cool, dry place.

  • SUGGESTED USE

    Take two (2) capsules daily, or as directed by your health care professional.

  • OTHER INGREDIENTS


    Vegetable Cellulose (from capsule), Rice Flour,Magnesium Sterate, and Silicon Dioxide.

  • Other Information

    Protect the product in this container from excessive heat and direct sun.

  • PRINCIPAL DISPLAY PANEL

    MOSS

  • INGREDIENTS AND APPEARANCE
    SEA MOSS DIETARY SUPPLEMENT 
    sea moss dietary supplement capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-996
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHONDRUS CRISPUS (UNII: OQS23HUA1X) (CHONDRUS CRISPUS - UNII:OQS23HUA1X) CHONDRUS CRISPUS350 mg  in 19445 mg
    CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL25 mg  in 19445 mg
    FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS100 mg  in 19445 mg
    CURCUMA LONGA WHOLE (UNII: W5488JUO8U) (CURCUMA LONGA WHOLE - UNII:W5488JUO8U) CURCUMA LONGA WHOLE100 mg  in 19445 mg
    WITHANIA SOMNIFERA FLOWER (UNII: 2HZ95R7082) (WITHANIA SOMNIFERA FLOWER - UNII:2HZ95R7082) WITHANIA SOMNIFERA FLOWER100 mg  in 19445 mg
    NIGELLA SATIVA SEED OIL (UNII: CS4U38E731) (NIGELLA SATIVA SEED OIL - UNII:CS4U38E731) NIGELLA SATIVA SEED OIL200 mg  in 19445 mg
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (ARCTIUM LAPPA ROOT - UNII:597E9BI3Z3) ARCTIUM LAPPA ROOT100 mg  in 19445 mg
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID90 mg  in 19445 mg
    Inactive Ingredients
    Ingredient NameStrength
    RICE BRAN (UNII: R60QEP13IC)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    ColorblueScoreno score
    ShapeCAPSULESize112mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-996-0119445 mg in 1 VIAL; Type 0: Not a Combination Product02/05/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/05/2024
    Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen XiaoMai Manufacturing Co., Ltd.712999147manufacture(83872-996)