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
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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
- Uses
- Warnings
- CAUTION
- When using this product
- Stop use and ask a doctor
- KEEP OUT OF THE REACH OF CHILDREN.
- SUGGESTED USE
- OTHER INGREDIENTS
- Other Information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SEA MOSS DIETARY SUPPLEMENT
sea moss dietary supplement capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-996 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHONDRUS CRISPUS (UNII: OQS23HUA1X) (CHONDRUS CRISPUS - UNII:OQS23HUA1X) CHONDRUS CRISPUS 350 mg in 19445 mg CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL 25 mg in 19445 mg FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 100 mg in 19445 mg CURCUMA LONGA WHOLE (UNII: W5488JUO8U) (CURCUMA LONGA WHOLE - UNII:W5488JUO8U) CURCUMA LONGA WHOLE 100 mg in 19445 mg WITHANIA SOMNIFERA FLOWER (UNII: 2HZ95R7082) (WITHANIA SOMNIFERA FLOWER - UNII:2HZ95R7082) WITHANIA SOMNIFERA FLOWER 100 mg in 19445 mg NIGELLA SATIVA SEED OIL (UNII: CS4U38E731) (NIGELLA SATIVA SEED OIL - UNII:CS4U38E731) NIGELLA SATIVA SEED OIL 200 mg in 19445 mg ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (ARCTIUM LAPPA ROOT - UNII:597E9BI3Z3) ARCTIUM LAPPA ROOT 100 mg in 19445 mg ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 90 mg in 19445 mg Inactive Ingredients Ingredient Name Strength RICE BRAN (UNII: R60QEP13IC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color blue Score no score Shape CAPSULE Size 112mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-996-01 19445 mg in 1 VIAL; Type 0: Not a Combination Product 02/05/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/05/2024 Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen XiaoMai Manufacturing Co., Ltd. 712999147 manufacture(83872-996)