Home NDC 55910-345 Headache Relief
Product NDC 55910-345
11-digit product format 559100345
Labeler code 55910
Product ID 55910-345_75ad20b0-987a-43b8-8fbd-f97c17410f01
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Aspirin, Caffeine
Dosage form TABLET, FILM COATED
Route ORAL
Labeler DOLGENCORP, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-05-06
Substance ACETAMINOPHEN; ASPIRIN; CAFFEINE
Active strength 250; 250; 65 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 Headache Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 250 mg/1 ASPIRIN 250 mg/1 CAFFEINE 65 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup R16CO5Y76E Internal UNII lookup 3G6A5W338E 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 55910-345-08 Headache Relief 1 in 1 CARTON TABLET, FILM COATED 1 8 55910-345-08 Headache Relief 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 8 55910-345-12 Headache Relief 1 in 1 CARTON TABLET, FILM COATED 1 8 55910-345-12 Headache Relief 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-345 HEADACHE RELIEF (ACETAMINOPHEN, ASPIRIN, CAFFEINE) TABLET, FILM COATED [DOLGENCORP, LLC] 7 Current NDC, Legacy NDC, 4 package rows 20240623_e1e24d52-0b4d-400b-8181-e3f6ab75c4f6.zip
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 Marketing end Sample Exclude flag Status 55910-345-08 55910034508 1 BOTTLE, PLASTIC in 1 CARTON (55910-345-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2021-05-06 0000-00-00 No No Current 55910-345-12 55910034512 1 BOTTLE, PLASTIC in 1 CARTON (55910-345-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2021-05-06 No No Current