Home NDC 0363-6693-80 Walgreens Headache Relief Extra Strength
Product NDC 0363-6693
Requested package NDC 0363-6693-80
11-digit product format 003636693
Labeler code 0363
Product ID 0363-6693_52109b65-3bf2-de38-e063-6394a90a9727
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen 250mg, Aspirin 250mg and Caffeine 65mg
Dosage form TABLET, COATED
Route ORAL
Labeler Walgreens
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-01
Substance CAFFEINE; ASPIRIN; ACETAMINOPHEN
Active strength 65; 250; 250 mg/1; mg/1; mg/1
Pharmacologic classes 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]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Walgreens Headache Relief Extra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 65 mg/1 ASPIRIN 250 mg/1 ACETAMINOPHEN 250 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3G6A5W338E Internal UNII lookup R16CO5Y76E Internal UNII lookup 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308297 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-6693-12 Walgreens Headache Relief Extra Strength 1 in 1 CARTON TABLET, COATED 1 1 0363-6693-12 Walgreens Headache Relief Extra Strength 120 in 1 BOTTLE, PLASTIC TABLET, COATED 120 1 0363-6693-20 Walgreens Headache Relief Extra Strength 20 in 1 BOTTLE, PLASTIC TABLET, COATED 20 1 0363-6693-20 Walgreens Headache Relief Extra Strength 1 in 1 CARTON TABLET, COATED 1 1 0363-6693-80 Walgreens Headache Relief Extra Strength 80 in 1 BOTTLE, PLASTIC TABLET, COATED 80 1 0363-6693-80 Walgreens Headache Relief Extra Strength 1 in 1 CARTON TABLET, COATED 1 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 0363-6693-80 00363669380 1 BOTTLE, PLASTIC in 1 CARTON (0363-6693-80) / 80 TABLET, COATED in 1 BOTTLE, PLASTIC 2026-05-01 No No Current