Label: 7030 CALCIUM PREMIUM- calcium capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 55259-2001-1 - Packager: Apexel Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 1, 2015
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
7030 CALCIUM PREMIUM
calcium capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55259-2001 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) ZINC OXIDE (UNII: SOI2LOH54Z) SELENIUM (UNII: H6241UJ22B) GERMANIUM (UNII: 00072J7XWS) IRON (UNII: E1UOL152H7) POTASSIUM (UNII: RWP5GA015D) MANGANESE (UNII: 42Z2K6ZL8P) Product Characteristics Color white (white) Score no score Shape OVAL (tablet) Size 12mm Flavor Imprint Code 3;hp;x Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55259-2001-1 120 in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/10/2013 Labeler - Apexel Co., Ltd (687287979) Registrant - Apexel Co., Ltd (687287979) Establishment Name Address ID/FEI Business Operations Apexel Co., Ltd 687287979 manufacture(55259-2001)