FDA.reportPublic FDA data

Lil Drug Store Pain Reliever

Product NDC
66715-9737
Requested package NDC
66715-9737-3
11-digit product format
667159737
Labeler code
66715
Product ID
66715-9737_ee1659ee-c88a-0d59-e053-2995a90a5a64
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Lil' Drug Store Products, Inc.
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-01-27
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage66715-973766715-9737-3DDiscontinued by firm2026-10-12

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 dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66715-9737-32024-01-30C16284748780-11030e365-181c-111a-e063-dadaa90a10e2Lil' Drug Store ® Pain Reliever Extra Strength
66715-9737-42024-01-30C16284748780-11030e365-181c-111a-e063-dadaa90a10e2Lil' Drug Store ® Pain Reliever Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66715-9737-3Lil Drug Store Pain Reliever Extra Strength2 in 1 POUCHTABLET27
66715-9737-3Lil Drug Store Pain Reliever Extra Strength3 in 1 CARTONTABLET37
66715-9737-4Lil Drug Store Pain Reliever Extra Strength10 in 1 VIALTABLET107

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AcetaminophenACTIVE INGREDIENT362O9ITL9DLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
AcetaminophenACTIVE MOIETY362O9ITL9DLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Cellulose, MicrocrystallineINACTIVE INGREDIENTOP1R32D61ULIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
HypromellosesINACTIVE INGREDIENT3NXW29V3WOLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
MaltodextrinINACTIVE INGREDIENT7CVR7L4A2DLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Polyethylene GlycolsINACTIVE INGREDIENT3WJQ0SDW1ALIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
PovidonesINACTIVE INGREDIENTFZ989GH94ELIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Sodium Starch Glycolate Type A CornINACTIVE INGREDIENTAG9B65PV6BLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Sodium Starch Glycolate Type A PotatoINACTIVE INGREDIENT5856J3G2A2LIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Starch, CornINACTIVE INGREDIENTO8232NY3SJLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Stearic AcidINACTIVE INGREDIENT4ELV7Z65APLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1
Titanium DioxideINACTIVE INGREDIENT15FIX9V2JPLIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66715-9737LIL DRUG STORE PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET [LIL' DRUG STORE PRODUCTS, INC.]7Legacy NDC, 3 package rows20221124_6ea4d4da-7463-4be8-a951-2164ec2d2904.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN6ea4d4da-7463-4be8-a951-2164ec2d29047
198440acetaminophen 500 MG Oral TabletSCD6ea4d4da-7463-4be8-a951-2164ec2d29047
198440APAP 500 MG Oral TabletSY6ea4d4da-7463-4be8-a951-2164ec2d29047

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66715-9737-3667159737033 POUCH in 1 CARTON (66715-9737-3) > 2 TABLET in 1 POUCH3 pouch2011-01-272021-08-30NoNoCurrent