Label: DR.NOAH MARUTOOTHPASTE- precipitated calcium carbonate paste
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Contains inactivated NDC Code(s)
NDC Code(s): 82359-0002-1 - Packager: DR.Noah
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 29, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNING
- USES
- INDICATION & USAGE SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.NOAH MARUTOOTHPASTE
precipitated calcium carbonate pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82359-0002 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 0.22 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82359-0002-1 120 g in 1 TUBE; Type 0: Not a Combination Product 10/29/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/29/2021 Labeler - DR.Noah (695333875) Registrant - DR.Noah (695333875) Establishment Name Address ID/FEI Business Operations DONG IL PHARMS CO., LTD. 557810721 manufacture(82359-0002) Establishment Name Address ID/FEI Business Operations DR.Noah 695333875 label(82359-0002)