pain reliever extra strength
Generic: acetaminophen, aspirin and caffeine
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
pain reliever extra strength
Generic Name
acetaminophen, aspirin and caffeine
Labeler
rite aid corporation
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 250 mg/1, aspirin 250 mg/1, caffeine 65 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
11822-1590
Product ID
11822-1590_5b83a208-7d51-432b-9afb-7c80556c1cfd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
1992-11-17
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118221590
Hyphenated Format
11822-1590
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
pain reliever extra strength (source: ndc)
Generic Name
acetaminophen, aspirin and caffeine (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
- 65 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-1590-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (11822-1590-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5b83a208-7d51-432b-9afb-7c80556c1cfd", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832", "N0000175739", "N0000175729", "N0000175790", "M0023046"], "upc": ["0011822317283"], "unii": ["362O9ITL9D", "R16CO5Y76E", "3G6A5W338E"], "rxcui": ["308297"], "spl_set_id": ["d9caee45-be43-45ec-927f-e7fec5c14f07"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]", "Xanthines [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]", "Central Nervous System Stimulation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]", "Central Nervous System Stimulant [EPC]", "Methylxanthine [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-1590-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-1590-2", "marketing_start_date": "19921117"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-1590-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-1590-8", "marketing_start_date": "19921117"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "11822-1590_5b83a208-7d51-432b-9afb-7c80556c1cfd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Methylxanthine [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]", "Xanthines [CS]"], "product_ndc": "11822-1590", "generic_name": "Acetaminophen, Aspirin and caffeine", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "ASPIRIN", "strength": "250 mg/1"}, {"name": "CAFFEINE", "strength": "65 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19921117", "listing_expiration_date": "20261231"}