quality choice extra strength effervescent antacid and pain relief
Generic: aspirin, anhydrous citric acid, sodium bicarbonate
Labeler: chain drug marketing associationDrug Facts
Product Profile
Brand Name
quality choice extra strength effervescent antacid and pain relief
Generic Name
aspirin, anhydrous citric acid, sodium bicarbonate
Labeler
chain drug marketing association
Dosage Form
TABLET, EFFERVESCENT
Routes
Active Ingredients
anhydrous citric acid 1000 mg/1, aspirin 500 mg/1, sodium bicarbonate 1985 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63868-569
Product ID
63868-569_26d1a02f-592c-5866-e063-6394a90a253e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2020-11-04
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868569
Hyphenated Format
63868-569
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
quality choice extra strength effervescent antacid and pain relief (source: ndc)
Generic Name
aspirin, anhydrous citric acid, sodium bicarbonate (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
- 500 mg/1
- 1985 mg/1
Packaging
- 12 POUCH in 1 CARTON (63868-569-24) / 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": "26d1a02f-592c-5866-e063-6394a90a253e", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089", "N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0635515997905"], "unii": ["XF417D3PSL", "R16CO5Y76E", "8MDF5V39QO"], "rxcui": ["1536833"], "spl_set_id": ["9f7d0c96-a561-a8a0-e053-2995a90a250b"], "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": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CARTON (63868-569-24) / 2 TABLET, EFFERVESCENT in 1 POUCH", "package_ndc": "63868-569-24", "marketing_start_date": "20201104"}], "brand_name": "Quality Choice Extra Strength Effervescent Antacid and Pain Relief", "product_id": "63868-569_26d1a02f-592c-5866-e063-6394a90a253e", "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": "63868-569", "generic_name": "Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Quality Choice Extra Strength Effervescent Antacid and Pain Relief", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "1000 mg/1"}, {"name": "ASPIRIN", "strength": "500 mg/1"}, {"name": "SODIUM BICARBONATE", "strength": "1985 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201104", "listing_expiration_date": "20261231"}