alka-seltzer cool action heartburn relief mint

Generic: calcium carbonate

Labeler: bayer healthcare llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alka-seltzer cool action heartburn relief mint
Generic Name calcium carbonate
Labeler bayer healthcare llc.
Dosage Form GUM, CHEWING
Routes
ORAL
Active Ingredients

calcium carbonate 750 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0001
Product ID 0280-0001_452374f2-bab8-ec4e-e063-6294a90adca9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2020-03-01

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02800001
Hyphenated Format 0280-0001

Supplemental Identifiers

RxCUI
2281777
UPC
0016500586074
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alka-seltzer cool action heartburn relief mint (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (0280-0001-01) / 8 GUM, CHEWING in 1 BLISTER PACK
  • 1 BLISTER PACK in 1 CARTON (0280-0001-02) / 8 GUM, CHEWING in 1 BLISTER PACK
  • 1 GUM, CHEWING in 1 POUCH (0280-0001-03)
  • 6 BLISTER PACK in 1 CARTON (0280-0001-04) / 10 GUM, CHEWING in 1 BLISTER PACK
source: ndc

Packages (4)

0280-0001-01 2 BLISTER PACK in 1 CARTON (0280-0001-01) / 8 GUM, CHEWING in 1 BLISTER PACK 0280-0001-02 1 BLISTER PACK in 1 CARTON (0280-0001-02) / 8 GUM, CHEWING in 1 BLISTER PACK 0280-0001-03 1 GUM, CHEWING in 1 POUCH (0280-0001-03) 0280-0001-04 6 BLISTER PACK in 1 CARTON (0280-0001-04) / 10 GUM, CHEWING in 1 BLISTER PACK

Ingredients (1)

calcium carbonate (750 mg/1)

Linked Drug Pages (1)

Alka-Seltzer Cool Action Heartburn Relief Mint ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "452374f2-bab8-ec4e-e063-6294a90adca9", "openfda": {"upc": ["0016500586074"], "unii": ["H0G9379FGK"], "rxcui": ["2281777"], "spl_set_id": ["9b8da147-8d0c-e6b0-e053-2a95a90a35e6"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0280-0001-01)  / 8 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0280-0001-01", "marketing_start_date": "20200301"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0280-0001-02)  / 8 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0280-0001-02", "marketing_start_date": "20200501"}, {"sample": false, "description": "1 GUM, CHEWING in 1 POUCH (0280-0001-03)", "package_ndc": "0280-0001-03", "marketing_start_date": "20200601"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0280-0001-04)  / 10 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "0280-0001-04", "marketing_start_date": "20241115"}], "brand_name": "Alka-Seltzer Cool Action Heartburn Relief Mint", "product_id": "0280-0001_452374f2-bab8-ec4e-e063-6294a90adca9", "dosage_form": "GUM, CHEWING", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "0280-0001", "generic_name": "Calcium Carbonate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Cool Action Heartburn Relief", "brand_name_suffix": "Mint", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "750 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}