Label: ULTRA STRENGTH NATURAL ANTACID- calcium carbonate tablet, chewable
- NDC Code(s): 30142-108-72
- Packager: KROGER COMPANY
- 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 August 23, 2023
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- Active ingredient (per tablet)
- Purpose
- Uses
- Warnings
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- When using this product
- Keep out of reach of children.
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- Inactive ingredients
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Package/Label Principal Display Panel
Kroger®
NDC# 30142-108-72
COMPARE TO the active ingredient in Ultra Strength TUMS®
*See back panel
Ultra Strength
Antacid Tablets
NATURALLY-DERIVED INGREDIENTS
Calcium Carbonate 1000 mg
FAST RELIEF: Upset Stomach, HeartburnandAcid Indigestion
Peppermint
Naturally Flavored
GLUTEN FREE
72 CHEWABLE TABLETS
Our Pharmacists Recommend
K PAREVE
DISTRIBUTED BY: THE KROGER CO. CINCINNATI, OHIO 45202
QUALITY GUARANTEE
800-632-6900
Tums® is a registered trademark of GlaxoSmithKline LLC, Warren, NJ 07059. GlaxoSmithKline LLC is not affiliated with The Kroger Co. or this product.
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INGREDIENTS AND APPEARANCE
ULTRA STRENGTH NATURAL ANTACID
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-108 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 1000 mg Inactive Ingredients Ingredient Name Strength DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) MALTODEXTRIN (UNII: 7CVR7L4A2D) PEPPERMINT (UNII: V95R5KMY2B) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876) Product Characteristics Color WHITE Score no score Shape ROUND Size 19mm Flavor PEPPERMINT Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-108-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 11/19/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 11/19/2019 Labeler - KROGER COMPANY (006999528)