alka-seltzer gold (0280-4100)

Drug Facts

Product Profile

Brand Name alka-seltzer gold

Generic Name alka-seltzer gold

Labeler bayer healthcare llc.

Dosage Form TABLET, EFFERVESCENT

Routes

ORAL

Active Ingredients

citric acid monohydrate 1000 mg/1, potassium bicarbonate 344 mg/1, sodium bicarbonate 1050 mg/1

Manufacturer

Bayer HealthCare LLC.

Identifiers & Regulatory

Product NDC 0280-4100

Product ID 0280-4100_4526b3d0-3667-afe5-e063-6294a90af3ab

Product Type HUMAN OTC DRUG

Marketing Category OTC MONOGRAPH DRUG

Application Number M001

Listing Expiration 2026-12-31

Marketing Start 2014-11-19

Pharmacologic Class

Classes

acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02804100

Hyphenated Format 0280-4100

Supplemental Identifiers

RxCUI

1536474

UPC

0016500041085

UNII

2968PHW8QP HM5Z15LEBN 8MDF5V39QO

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 gold (source: ndc)

Generic Name alka-seltzer gold (source: ndc)

Application Number M001 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1000 mg/1
344 mg/1
1050 mg/1

source: ndc

Packaging

18 POUCH in 1 CARTON (0280-4100-63) / 2 TABLET, EFFERVESCENT in 1 POUCH

source: ndc

Packages (1)

0280-4100-63 18 POUCH in 1 CARTON (0280-4100-63) / 2 TABLET, EFFERVESCENT in 1 POUCH

Ingredients (3)

citric acid monohydrate (1000 mg/1) potassium bicarbonate (344 mg/1) sodium bicarbonate (1050 mg/1)

Linked Drug Pages (1)

Alka-Seltzer Gold ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "4526b3d0-3667-afe5-e063-6294a90af3ab", "openfda": {"upc": ["0016500041085"], "unii": ["2968PHW8QP", "HM5Z15LEBN", "8MDF5V39QO"], "rxcui": ["1536474"], "spl_set_id": ["0824bedb-413b-2fa0-e054-00144ff88e88"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (0280-4100-63)  / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "0280-4100-63", "marketing_start_date": "20141119"}], "brand_name": "Alka-Seltzer Gold", "product_id": "0280-4100_4526b3d0-3667-afe5-e063-6294a90af3ab", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0280-4100", "generic_name": "Alka-Seltzer Gold", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Gold", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": "1000 mg/1"}, {"name": "POTASSIUM BICARBONATE", "strength": "344 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1050 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20141119", "listing_expiration_date": "20261231"}