Label: UP AND UP ULTRA STRENGTH ANTACID 1000- calcium carbonate tablet, chewable
- NDC Code(s): 82442-101-72
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 7, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (per tablet)
- Purpose
- Uses
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Warnings
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
• do not take more than 7 tablets in 24 hours
• if pregnant do not take more than 5 tablets in 24 hours
• do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor - Directions
- Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
Compare to active ingredient in Tums Ultra®*
TROPICAL FRUIT FLAVOR
naturally and artificially flavored
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.
Distributed by
Target Corp.
Mpls., MN 55403
Made in India
TM & ©2023 Target Brands, Inc.*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength TUMS®.
- Packaging
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INGREDIENTS AND APPEARANCE
UP AND UP ULTRA STRENGTH ANTACID 1000
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82442-101 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 1000 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color white, yellow, orange, pink Score no score Shape ROUND Size 19mm Flavor FRUIT (TROPICAL FRUIT FLAVOR) Imprint Code VB101 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-101-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 04/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 04/07/2023 Labeler - Target Corporation (006961700) Registrant - VIRCHOW BIOTECH PRIVATE LIMITED (737786315) Establishment Name Address ID/FEI Business Operations VIRCHOW BIOTECH PRIVATE LIMITED 737786315 manufacture(82442-101)
