Home NDC 11822-6451 pain relief aspirin
Product NDC 11822-6451
11-digit product format 118226451
Labeler code 11822
Product ID 11822-6451_6112edb9-72ca-4744-a62a-aafdf411eeda
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Rite Aid Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-07-25
Substance ASPIRIN
Active strength 81 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 pain relief aspirin
Brand name suffix Low Dose
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308416 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 11822-6451-1 pain relief aspirinLow Dose 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 14 11822-6451-1 pain relief aspirinLow Dose 1 in 1 CARTON TABLET, DELAYED RELEASE 1 14 11822-6451-4 pain relief aspirinLow Dose 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 14 11822-6451-6 pain relief aspirinLow Dose 1 in 1 CARTON TABLET, DELAYED RELEASE 1 14 11822-6451-6 pain relief aspirinLow Dose 200 in 1 BOTTLE TABLET, DELAYED RELEASE 200 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 ASPIRIN ACTIVE MOIETY R16CO5Y76E PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 METHACRYLIC ACID INACTIVE INGREDIENT 1CS02G8656 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 TALC INACTIVE INGREDIENT 7SEV7J4R1U PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, COATED [RITE AID] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-6451 PAIN RELIEF ASPIRIN LOW DOSE (ASPIRIN) TABLET, DELAYED RELEASE [RITE AID CORPORATION] 13 Current NDC, Legacy NDC, 5 package rows 20240829_df7835c9-f10f-40c6-8955-61423d94b677.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 Units Marketing start Marketing end Sample Exclude flag Status 11822-6451-1 11822645101 1 BOTTLE, PLASTIC in 1 CARTON (11822-6451-1) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2014-07-25 No No Current 11822-6451-4 11822645104 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11822-6451-4) 2014-07-25 0000-00-00 No No Current 11822-6451-6 11822645106 1 BOTTLE in 1 CARTON (11822-6451-6) > 200 TABLET, COATED in 1 BOTTLE 1 bottle 2014-07-25 0000-00-00 No No Current