Home NDC 69968-0793-01 NDC 69968-0793-01 - Tylenol Precise Cooling Pain Relieving 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 69968-0793
Requested NDC 69968-0793-01
Package NDCs from labels 69968-0793-1, 69968-0793-4, 69968-0793-9, 69968-0793-2, 69968-0793-01
Manufacturer Kenvue Brands LLC
Effective date 2026-02-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0793-1 Tylenol Precise Cooling Pain Relieving 14.2 g in 1 TUBE CREAM 14.2 5 69968-0793-1 Tylenol Precise Cooling Pain Relieving 1 in 1 CARTON CREAM 1 5 69968-0793-2 Tylenol Precise Cooling Pain Relieving 1 in 1 CARTON CREAM 1 5 69968-0793-2 Tylenol Precise Cooling Pain Relieving 70 g in 1 TUBE CREAM 70 5 69968-0793-4 Tylenol Precise Cooling Pain Relieving 113 g in 1 TUBE CREAM 113 5 69968-0793-4 Tylenol Precise Cooling Pain Relieving 1 in 1 CARTON CREAM 1 5 69968-0793-9 Tylenol Precise Cooling Pain Relieving 113 g in 1 TUBE CREAM 113 5 69968-0793-9 Tylenol Precise Cooling Pain Relieving 2 in 1 CARTON CREAM 2 5 69968-0793-1 TYLENOL Extra Strength / TYLENOL Precise Cooling Pain Relief 1 in 1 CARTON CREAM 40 mg in 1g 1 69968-0793-1 TYLENOL Extra Strength / TYLENOL Precise Cooling Pain Relief 14.2 g in 1 TUBE CREAM 14.2 g 40 mg in 1g 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0793 TYLENOL PRECISE COOLING PAIN RELIEVING (LIDOCAINE, MENTHOL) CREAM [KENVUE BRANDS LLC] 4 Current NDC, 8 package rows 20250303_fc0a3404-b174-3952-e053-6294a90a1e02.zip 69968-0793 TYLENOL EXTRA STRENGTH / TYLENOL PRECISE COOLING PAIN RELIEF (ACETAMINOPHEN, LIDOCAINE, MENTHOL) KIT [KENVUE BRANDS LLC] 1 Current NDC 20241204_2611e984-0dd5-bda1-e063-6394a90a559a.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 34 of 521 · 10,419 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Sinus Congestion and Pain Maximum Strength ACETAMINOPHEN, PHENYLEPHRINE HCL Rugby Laboratories fc42e97d-1224-4d29-a55d-1a1885e0bf8f 2026-07-09 Warnings Exact identifier unii: 362O9ITL9D Aspirin Regular Strength ASPIRIN FOODHOLD U.S.A., LLC 9e09b4fb-e015-45ea-8b1c-27faf65572aa 2026-07-09 Warnings Exact identifier application number: M013 Tension Headache Relief ACETAMINOPHEN, CAFFEINE Walgreen Company f13fb7e9-50ea-4e2c-a442-38b1b5b315d7 2026-07-09 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Head Congestion and Mucus ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL Cardinal Health 110, LLC. DBA Leader 7418d92d-a540-40d6-91d0-b7eb1f87f8ff 2026-07-08 Warnings Exact identifier unii: 362O9ITL9D Bombee Honey Daily Glow Shield Sunscreen HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE ABT ASIA Inc. 56112dff-b091-7a56-e063-6294a90a77d3 2026-07-08 Warnings Exact identifier unii: 15FIX9V2JP Acetaminophen 500 Pyrilamine Maleate 15 and Caffeine 60 ACETAMINOPHEN 500MG PYRILAMINE MALEATE 15MG AND CAFFEINE 60MG TABLETS Health Pharma USA LLC 34eb8a9b-d0ee-13e8-e063-6294a90a2fef 2026-07-08 Warnings Exact identifier application number: M013 Acetaminophen 250 mg Aspirin 250 mg Caffeine 65 mg ACETAMINOPHEN 250 MG ASPIRIN 250 MG CAFFEINE 65 MG Health Pharma USA LLC 3590d417-272b-ae4d-e063-6394a90a5dc6 2026-07-08 Warnings Exact identifier application number: M013 Nupharmisto 4% Lidocaine Numbing cream LIDOCAINE 4% EveryMarket Inc 5615e49d-e03b-f915-e063-6294a90a1786 2026-07-08 Warnings Exact identifier application number: M017 unii: 98PI200987 GOODMEDS EXTRA STRENGTH PAIN RELIEF ACETAMINOPHEN ACETAMINOPHEN Cabinet Health P.B.C. 88884253-5a79-4ac1-b8ce-03966d8b509d 2026-07-08 Warnings Exact identifier application number: M013 rxcui: 198440 unii: 362O9ITL9D Freskaro Ear Drops for Swimmers FRESKARO EAR DROPS FOR SWIMMERS Pharma Nobis, LLC 4f724d85-cd38-41da-e063-6394a90a9fd7 2026-07-08 Warnings Exact identifier unii: PDC6A3C0OX CAREALL Musle and Joint MENTHOL New World Imports, Inc 561cc103-ae88-8f30-e063-6294a90a05c4 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A HealthWise Medicated Cold Hot MENTHOL Veridian Healthcare, LLC 561e1409-d1d8-e35d-e063-6394a90a4d8f 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Natures Willow Balm Roll On Pain Relief MENTHOL WB Ventures LLC 3b1834e6-75cd-5380-e063-6294a90ad1d5 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Natures Willow Balm Itch Relief Cream MENTHOL WB Ventures LLC 0ce31b5d-4401-460c-e063-6394a90ab558 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A CAREALL Hydrocortisone Maximum Strength HYDROCORTISONE New World Imports, Inc. 560a4abf-31dd-333f-e063-6294a90a3505 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Balm MENTHOL WB VENTURES LLC b9f50c43-b0d5-39a8-e053-2995a90a04f1 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Natures Willow Bug Bite Balm MENTHOL WB Ventures LLC b9fab18f-32c7-d5bd-e053-2995a90a6d0f 2026-07-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Welmate Numbing Relief LIDOCAINE 5% YYBA Corp 562162c0-7a85-f83c-e063-6294a90a8fc5 2026-07-08 Warnings Exact identifier unii: 98PI200987 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 DERMIO DERMATOLOGY LLC 562f5b0d-6a10-305d-e063-6394a90a5980 2026-07-08 Warnings Exact identifier unii: 15FIX9V2JP Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 Suzanne's Skin2soul LLC 562fbaa6-f93a-5ec4-e063-6294a90a9634 2026-07-08 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.