Label: HEB ANTACID CALCIUM ASSORTED BERRY- calcium carbonate tablet, chewable
- NDC Code(s): 37808-103-28
- Packager: HEB
- 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 September 21, 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
H-E-B®
NDC# 37808-103-28
Compare To Ultra Strength Tums® active ingredient*
ULTRA STRENGTH
Antacid Tablets
CALCIUM CARBONATE 1000 mg/Antacid
RELIEF OF:
- •
- Acid Indigestion
- •
- Sour Stomach
- •
- Heartburn
Assorted Berry Flavors
GLUTEN FREE
265 CHEWABLE TABLETS
K PAREVE
100% GUARANTEE promise
MADE WITH PRIDE & CARE FOR H-E-B® SAN ANTONIA, TX 78204
*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength Tums®.
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INGREDIENTS AND APPEARANCE
HEB ANTACID CALCIUM ASSORTED BERRY
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-103 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 ADIPIC ACID (UNII: 76A0JE0FKJ) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color RED, PINK, PURPLE, BLUE Score no score Shape ROUND Size 19mm Flavor BERRY (assorted berry) Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-103-28 265 in 1 BOTTLE; Type 0: Not a Combination Product 02/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 02/20/2019 Labeler - HEB (007924756)