alka-seltzer ultra strength heartburn reliefchews strawberry and orange

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 ultra strength heartburn reliefchews strawberry and orange
Generic Name calcium carbonate
Labeler bayer healthcare llc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-0059
Product ID 0280-0059_45262db7-ea04-6c50-e063-6394a90a025d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-03-03

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 02800059
Hyphenated Format 0280-0059

Supplemental Identifiers

RxCUI
308892
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 ultra strength heartburn reliefchews strawberry and orange (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0059-50)
source: ndc

Packages (1)

0280-0059-50 50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0059-50)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orange ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45262db7-ea04-6c50-e063-6394a90a025d", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["84771ac5-ad0b-e0ec-e053-2a91aa0a1b36"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0280-0059-50)", "package_ndc": "0280-0059-50", "marketing_start_date": "20190303"}], "brand_name": "Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orange", "product_id": "0280-0059_45262db7-ea04-6c50-e063-6394a90a025d", "dosage_form": "TABLET, CHEWABLE", "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": "0280-0059", "generic_name": "Calcium Carbonate", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Ultra Strength Heartburn ReliefChews", "brand_name_suffix": "Strawberry and Orange", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190303", "listing_expiration_date": "20261231"}