Pain Reliever

Product NDC
11822-6440
11-digit product format
118226440
Labeler code
11822
Product ID
11822-6440_23fc9191-f012-4087-95d0-af77f35e5434
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
LIQUID
Route
ORAL
Labeler
Rite Aid Corporation
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-31
Marketing end
2026-05-29
Substance
ACETAMINOPHEN
Active strength
500 mg/15mL
NDC exclude flag
No
Current FDA listing
Yes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-6440-12023-02-20C16284748780-1d6a99b39-3a8e-a426-e053-dadaa90af4c2Drug Facts
11822-6440-12022-01-28C16284748780-1d6a99b39-3a8e-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-6440-1Pain RelieverExtra Strength237 mL in 1 BOTTLE, PLASTICLIQUID2374

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-6440PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) LIQUID [RITE AID CORPORATION]3Current NDC, Legacy NDC, 1 package rows20240503_b628a3d1-4534-453c-ac5a-573325662ddc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-6440-111822644001237 mL in 1 BOTTLE, PLASTIC (11822-6440-1) 237 ml2020-01-312026-05-29NoNoCurrent