Label: ALKA-SELTZER HEARTBURN RELIEFCHEWS- calcium carbonate tablet, chewable
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NDC Code(s):
0280-0221-01,
0280-0221-02,
0280-0221-03,
0280-0221-08, view more0280-0221-12, 0280-0221-36, 0280-0221-60, 0280-0221-90
- Packager: Bayer HealthCare LLC.
- 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 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each chewable 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.
- Directions
- Other information
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Inactive ingredients
acacia, beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, DL-alpha tocopherol, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #5 lake (tartrazine), FD&C yellow #6, FD&C yellow #6 aluminum lake, FD&C yellow #6 lake, flavors, hydrogenated coconut oil, medium chain triglycerides, methyl paraben, modified starch, phosphoric acid, pregelatinized modified starch, propyl paraben, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 36 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
ALKA-SELTZER HEARTBURN RELIEFCHEWS
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0280-0221 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 750 mg Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) ACACIA (UNII: 5C5403N26O) CARNAUBA WAX (UNII: R12CBM0EIZ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) STARCH, CORN (UNII: O8232NY3SJ) CORN SYRUP (UNII: 9G5L16BK6N) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) ALUMINUM OXIDE (UNII: LMI26O6933) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) METHYLPARABEN (UNII: A2I8C7HI9T) PHOSPHORIC ACID (UNII: E4GA8884NN) PROPYLPARABEN (UNII: Z8IX2SC1OH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SHELLAC (UNII: 46N107B71O) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBIC ACID (UNII: X045WJ989B) SORBITOL (UNII: 506T60A25R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SUCROSE (UNII: C151H8M554) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color yellow, orange, pink Score no score Shape ROUND Size 18mm Flavor LEMON, ORANGE, STRAWBERRY Imprint Code AS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0280-0221-36 36 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2014 2 NDC:0280-0221-60 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2014 3 NDC:0280-0221-12 120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/15/2014 4 NDC:0280-0221-90 90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/12/2015 5 NDC:0280-0221-08 8 in 1 POUCH; Type 0: Not a Combination Product 03/23/2016 6 NDC:0280-0221-01 32 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2020 7 NDC:0280-0221-02 66 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2020 8 NDC:0280-0221-03 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/15/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 03/15/2014 Labeler - Bayer HealthCare LLC. (112117283)