alka-seltzer original
Generic: anhydrous citric acid, aspirin, and sodium bicarbonate
Labeler: select consumer groupDrug Facts
Product Profile
Brand Name
alka-seltzer original
Generic Name
anhydrous citric acid, aspirin, and sodium bicarbonate
Labeler
select consumer group
Dosage Form
TABLET, EFFERVESCENT
Routes
Active Ingredients
anhydrous citric acid 1000 mg/1, aspirin 325 mg/1, sodium bicarbonate 1916 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
85237-1829
Product ID
85237-1829_3ca80d7c-b154-7abf-e063-6294a90ae6bb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2010-03-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
852371829
Hyphenated Format
85237-1829
Supplemental Identifiers
RxCUI
UNII
NUI
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 original (source: ndc)
Generic Name
anhydrous citric acid, aspirin, and sodium bicarbonate (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
- 325 mg/1
- 1916 mg/1
Packaging
- 1 POUCH in 1 BLISTER PACK (85237-1829-1) / 2 TABLET, EFFERVESCENT in 1 POUCH
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ca80d7c-b154-7abf-e063-6294a90ae6bb", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089", "N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "unii": ["XF417D3PSL", "R16CO5Y76E", "8MDF5V39QO"], "rxcui": ["1536675", "1536680"], "spl_set_id": ["3ca80d74-1e8b-49d9-e063-6394a90a4312"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]", "Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]", "Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Select Consumer Group"]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 BLISTER PACK (85237-1829-1) / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "85237-1829-1", "marketing_start_date": "20100302"}], "brand_name": "Alka-Seltzer Original", "product_id": "85237-1829_3ca80d7c-b154-7abf-e063-6294a90ae6bb", "dosage_form": "TABLET, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Alkalinizing Activity [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Coagulation Factor Activity [PE]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "85237-1829", "generic_name": "ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE", "labeler_name": "Select Consumer Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Original", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "1000 mg/1"}, {"name": "ASPIRIN", "strength": "325 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1916 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100302", "listing_expiration_date": "20261231"}