Label: HANTAI 8030 CA-D3 GOLD (ostreae concha- calcium 99% tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 55259-0004-1 - Packager: APEXEL CO., LTD.
- 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 March 17, 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 INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNING
- Please note it may choke during the intake tablets.
- Please check product ingredients if you have any allergies before taking.
- Please be careful during open the product package.
- Keep product out of direct sunlight, high temperature and humidity.
- Store in a cool dry place.
- Keep out of reach of children.
- Any items past the expiration date or damaged in transit can be exchanged where you originally purchased the item.
- USES
- INDICATION & USAGE SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HANTAI 8030 CA-D3 GOLD
ostreae concha (calcium 99%) tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55259-0004 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM (UNII: SY7Q814VUP) (CALCIUM - UNII:SY7Q814VUP) CALCIUM 0.99 Inactive Ingredients Ingredient Name Strength MAGNESIUM (UNII: I38ZP9992A) MANGANESE (UNII: 42Z2K6ZL8P) GERMANIUM (UNII: 00072J7XWS) IRON (UNII: E1UOL152H7) POTASSIUM (UNII: RWP5GA015D) ZINC OXIDE (UNII: SOI2LOH54Z) SELENIUM (UNII: H6241UJ22B) Product Characteristics Color white Score score with uneven pieces Shape OVAL Size 12mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55259-0004-1 1 in 1 PACKAGE 03/18/2021 1 120 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/18/2021 Labeler - APEXEL CO., LTD. (687287979) Registrant - APEXEL CO., LTD. (687287979) Establishment Name Address ID/FEI Business Operations APEXEL CO., LTD. 687287979 manufacture(55259-0004)