Up And Up Ultra Strength Antacid 1000
FDA Label NDC 82442-101
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Up And Up Ultra Strength Antacid 1000 (NDC 82442-101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient (per tablet), purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient (Per Tablet)
Calcium Carbonate USP 1000mg
Purpose
Antacid
Uses
relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms
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
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
• adults and children 12 years of age and over: chew 2-3 tablets completely as symptoms occur, or as directed by a doctor. Do not swallow tablets whole.
• do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
Other Information
• each tablet contains: calcium 400mg
• store at controlled room temperature. Keep the container tightly closed.
Inactive Ingredients
adipic acid, D&C Yellow No.10 Lake, dextrose, FD&C Red No. 40 Lake, FD&C Yellow No. 6 Lake, flavors, magnesium stearate, maltodextrin, starch, sucralose.
Questions Or Comments?
call 1-800-910-6874
Packaging
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