Label: ALKA-SELTZER ULTRA STRENGTH HEARTBURN RELIEFCHEWS- calcium carbonate tablet, chewable
- NDC Code(s): 0280-0245-50
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Uses
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WARNINGS
Warnings
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other
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INACTIVE INGREDIENT
Inactive ingredients acacia, annatto extract, ascorbyl palmitate, beta carotene, carnauba wax, citric acid, confectioners sugar, corn syrup, disodium EDTA, dl-alpha-Tocopherol, FD&C Red #40 aluminum lake, FD&C Yellow #6 aluminum lake, flavors, hydrogenated coconut oil, lecithin, maltodextrin, methylparaben, modified starch, potassium hydroxide, potassium sorbate, propylene glycol, propylparaben, shellac, silicon dioxide, sodium ascorbate, sorbic acid, sorbitol, sugar, titanium dioxide, turmeric oleoresin, vegetable oil, water, white wax
- QUESTIONS
- Package label 50 count
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INGREDIENTS AND APPEARANCE
ALKA-SELTZER ULTRA STRENGTH HEARTBURN RELIEFCHEWS
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0280-0245 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 SHELLAC (UNII: 46N107B71O) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TURMERIC (UNII: 856YO1Z64F) ANNATTO (UNII: 6PQP1V1B6O) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) MALTODEXTRIN (UNII: 7CVR7L4A2D) SODIUM ASCORBATE (UNII: S033EH8359) WATER (UNII: 059QF0KO0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) ASCORBYL PALMITATE (UNII: QN83US2B0N) SUNFLOWER OIL (UNII: 3W1JG795YI) STARCH, POTATO (UNII: 8I089SAH3T) COCONUT OIL (UNII: Q9L0O73W7L) CORN OIL (UNII: 8470G57WFM) PALM OIL (UNII: 5QUO05548Z) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SORBIC ACID (UNII: X045WJ989B) SORBITOL (UNII: 506T60A25R) ACACIA (UNII: 5C5403N26O) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM) WHITE WAX (UNII: 7G1J5DA97F) CARNAUBA WAX (UNII: R12CBM0EIZ) .BETA.-CAROTENE (UNII: 01YAE03M7J) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) CORN SYRUP (UNII: 9G5L16BK6N) METHYLPARABEN (UNII: A2I8C7HI9T) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SUCROSE (UNII: C151H8M554) Product Characteristics Color yellow, orange Score no score Shape ROUND Size 18mm Flavor MANGO, PEACH, TROPICAL FRUIT PUNCH Imprint Code U2 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0280-0245-50 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 03/01/2017 Labeler - Bayer HealthCare LLC. (112117283)