FDA.reportPublic FDA data

NDC 70000-0171-06 - Leader All Day Pain Relief

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70000-0171
Requested NDC
70000-0171-06
Package NDCs from labels
70000-0171-1, 70000-0171-2, 70000-0171-3, 70000-0171-4, 70000-0171-5, 70000-0171-6, 70000-0171-06
Manufacturer
Cardinal Health 110, LLC. dba Leader
Effective date
2026-01-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Leader All Day Pain Relief - Cardinal Health 110, LLC. dba LeaderCardinal Health 110, LLC. dba Leader2026-01-26HUMAN OTC DRUG LABEL
Cardinal Health All Day Pain Relief Drug FactsRPK Pharmaceuticals, Inc.2023-06-07HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70000-0171-1Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-1Leader All Day Pain Relief100 in 1 BOTTLETABLET, FILM COATED10012
70000-0171-2Leader All Day Pain Relief200 in 1 BOTTLETABLET, FILM COATED20012
70000-0171-2Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-3Leader All Day Pain Relief50 in 1 BOTTLETABLET, FILM COATED5012
70000-0171-3Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-4Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-4Leader All Day Pain Relief120 in 1 BOTTLETABLET, FILM COATED12012
70000-0171-5Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-5Leader All Day Pain Relief24 in 1 BOTTLETABLET, FILM COATED2412
70000-0171-6Leader All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
70000-0171-6Leader All Day Pain Relief90 in 1 BOTTLETABLET, FILM COATED9012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70000-0171LEADER ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [CARDINAL HEALTH 110, LLC. DBA LEADER]11Current NDC, Legacy NDC, 12 package rows20250209_dbf007f5-c792-43a7-8cc1-bfa617f3a7fa.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0171-1EA - Each70000-0171e05656d5-33d1-40ba-9751-644da0178ad812017-08-11
70000-0171-2EA - Each70000-0171789cc451-c6fa-4332-9939-93e0d048d9e512019-01-24
70000-0171-3EA - Each70000-0171d59353bf-0052-43df-a9e2-e8584035e66b12019-01-24
70000-0171-4EA - Each70000-01714c328d8e-b3fb-4cb0-9edf-4e8f036448d112018-03-08
70000-0171-5EA - Each70000-017169b500c6-90e7-45fc-b5a9-d1fe94a8826712022-06-06
70000-0171-6EA - Each70000-0171219a944c-aabf-4166-a743-7855e87d213c12022-11-07

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 2 of 120 · 2,392 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30CORBY, JR., TERRY L.594443fd-8e27-4ec6-e063-6294a90a3ff02026-08-17WarningsExact identifier
unii: 15FIX9V2JP
Leader Dry Eye Relief Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400CARDINAL HEALTH 110, LLC. DBA LEADER2ded4bda-b3c3-4521-8701-5c8446fd148b2026-08-17WarningsExact identifier
unii: 3NXW29V3WO
NaproxenNAPROXEN SODIUML.N.K. International, Inc.82412133-c11a-4905-a119-965f44de10b72026-08-17WarningsExact identifier
rxcui: 849574
unii: 9TN87S3A3C
Naproxen SodiumNAPROXEN SODIUMHarris Teeter27938b08-ff37-4587-aa81-5ec3ef21a28a2026-08-12WarningsExact identifier
rxcui: 849574
unii: 9TN87S3A3C
Naproxen SodiumNAPROXEN SODIUMHarris Teeter38543976-ccbe-4af9-b01d-ae102452d4182026-08-12WarningsExact identifier
rxcui: 849574
unii: 9TN87S3A3C
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DR. SAMRAO'S OFFICE58b2ca35-11ed-d848-e063-6294a90a5b372026-08-11WarningsExact identifier
unii: 15FIX9V2JP
Dr. Shitong Photon Energy Eye Care LiquidTETRAHYDROZOLINE HCL 0.05% HYPROMELLOSE 0.3% DR. SHITONG PHOTON ENERGY EYE CARE LIQUIDWenzhou Yuyuan Pharmaceutical Co., Ltd.58ace434-55ef-17ef-e063-6294a90aa8782026-08-10WarningsExact identifier
unii: 3NXW29V3WO
Journee Firm Riche Broad Spectrum Sunscreen SPF 30TITANIUM DIOXIDE AND ZINC OXIDEMerz North America, Inc.d4d4bfcf-3674-4847-8ad8-1716a8e821ae2026-08-10WarningsExact identifier
unii: 15FIX9V2JP
VEIRFOO Brightening Hydrating Antiwrinkle SunscreenTITANIUM DIOXIDE, OCTINOXATELCM TECHNOLOGY Co., Ltd4cbbf8aa-8910-b7e7-e063-6294a90a4f072026-08-07WarningsExact identifier
unii: 15FIX9V2JP
Naproxen SodiumNAPROXEN SODIUMBryant Ranch Prepackbee7b482-8ba5-411d-90ee-de00df50d2b72026-08-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9TN87S3A3C
Naproxen SodiumNAPROXEN SODIUMBryant Ranch Prepacke9eb8c40-85d9-4c8e-9523-a21d3591260f2026-08-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 9TN87S3A3C
EltaMD UV RestoreTITANIUM DIOXIDE, ZINC OXIDE SUNSCREENCP Skin Health Group, Inc37fee381-ce6b-4949-9a4a-778aa839fb842026-08-06WarningsExact identifier
unii: 15FIX9V2JP
ArtridolNAPROXEN SODIUMZapotol Products Corpc422d300-3f4e-4121-8eaf-56683911b8842026-08-05WarningsExact identifier
rxcui: 849574
unii: 9TN87S3A3C
Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEYOCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8%Lale Cosmetics LLC581fb0cd-c55d-d562-e063-6394a90a7f112026-08-03WarningsExact identifier
unii: 15FIX9V2JP
EltaMD UV ActiveZINC OXIDE AND TITANIUM DIOXIDE SUNSCREENCP Skin Health Group, Inc39d16479-d491-4c19-aa11-674461687c7b2026-08-03WarningsExact identifier
unii: 15FIX9V2JP
Continuous Correction CreamTITANIUM DIOXIDEBaxter of California, LLC1cbcc648-f2e1-af60-e063-6294a90ad4bb2026-07-31WarningsExact identifier
unii: 15FIX9V2JP
Cover CremeTITANIUM DIOXIDEBaxter of California31f5e8c4-523f-4596-e063-6294a90a6a122026-07-31WarningsExact identifier
unii: 15FIX9V2JP
Good Sense Naproxen SodiumNAPROXEN SODIUMPreferred Pharmaceuticals Inc.2183df53-ac90-4d43-8a5d-8421036bc4cb2026-07-28WarningsExact identifier
application number: ANDA074661
rxcui: 849574
unii: 9TN87S3A3C
NaproxenNAPROXEN SODIUMPreferred Pharmaceuticals, Inc.20eb9d9f-11df-464f-a1b0-949f8fda40422026-07-28WarningsExact identifier
rxcui: 849574
unii: 9TN87S3A3C
Naproxen SodiumNAPROXEN SODIUMPD-Rx Pharmaceuticals, Inc.d2b1eedb-2be0-42af-ba0b-9da98560c91e2026-07-24WarningsExact identifier
application number: ANDA074661
rxcui: 849574
unii: 9TN87S3A3C

Reported adverse events (FAERS/openFDA)#

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