Home NDC 69968-0223-01 NDC 69968-0223-01 - Johnson and Johnson All Purpose First Aid Kit 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 69968-0223
Requested NDC 69968-0223-01
Package NDCs from labels 69968-0223-1, 69968-0223-2, 69968-0223-01
Manufacturer Kenvue Brands LLC
Effective date 2025-11-06
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 69968-0223-1 Benadryl Extra StrengthItch Stopping 1 in 1 CARTON CREAM 1 10 69968-0223-1 Benadryl Extra StrengthItch Stopping 28.3 g in 1 TUBE CREAM 28.3 10 69968-0223-2 Benadryl Extra StrengthItch Stopping 28.3 g in 1 TUBE CREAM 28.3 10 69968-0223-1 Johnson and Johnson All Purpose First Aid Kit 28.3 g in 1 TUBE CREAM 28.3 g 20 mg in 1g 7 69968-0223-1 Johnson and Johnson All Purpose First Aid Kit 1 in 1 CARTON CREAM 1 mg in 1g 7 69968-0223-1 Johnson and Johnson First Aid All Purpose160 CT 1 in 1 CARTON CREAM 20 mg in 1g 3 69968-0223-1 Johnson and Johnson First Aid All Purpose160 CT 28.3 g in 1 TUBE CREAM 28.3 g 1 mg in 1g 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0223 BENADRYL EXTRA STRENGTH ITCH STOPPING (DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE) CREAM [KENVUE BRANDS LLC] 10 Current NDC, Legacy NDC, 3 package rows 20241116_a1c1b878-d58f-41ff-b7a8-477f28c52667.zip 69968-0223 JOHNSON AND JOHNSON ALL PURPOSE FIRST AID KIT (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] 6 Current NDC, Legacy NDC 20241116_5cdb47c5-7951-4279-8a05-0a3199d3dd45.zip 69968-0223 JOHNSON AND JOHNSON FIRST AID ALL PURPOSE 160 CT (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] 2 Current NDC, Legacy NDC 20241116_f3933330-2550-4a88-e053-2a95a90a3997.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 9 of 630 · 12,591 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Daytime Cold and Flu Maximum Strength ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL Shield Pharmaceuticals Corp 67849e09-2056-4013-98b1-d003ed3250a2 2026-08-31 Warnings Exact identifier unii: 362O9ITL9D MAX relief junior ACETAMINOPHEN Akron Pharma Inc. 0e43b885-3843-4f11-9a53-02a38c228313 2026-08-31 Warnings Exact identifier application number: M013 unii: 362O9ITL9D MAX relief junior CHILDREN ACETAMINOPHEN Akron Pharma Inc. d7874e4d-0b38-4bb1-9a62-aa4f66d9baf9 2026-08-31 Warnings Exact identifier application number: M013 unii: 362O9ITL9D MAX relief junior Grape CHILDREN ACETAMINOPHEN Akron Pharma Inc. 3c7a7f40-4963-4fd1-942e-93fa08a45830 2026-08-31 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Genexa Kids Pain and Fever ACETAMINOPHEN Genexa Inc. 5a615118-33c9-1520-e063-6394a90a21a6 2026-08-31 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Itch Stopping DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE HyVee Inc 53157137-b980-45d2-aa10-8c111c0ec2f4 2026-08-31 Warnings Exact identifier application number: M017 rxcui: 1087026 unii: FM5526K07A unii: TC2D6JAD40 triple antibiotic BACITRACIN ZINC, NEOMYCIN, POLYMYXIN B Walgreen Company 4f3cfe39-2df8-48b4-954d-5997217c92ba 2026-08-31 Warnings Exact identifier unii: 057Y626693 unii: 19371312D4 Acetaminophen PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL United Natural Foods, Inc. dba UNFI 24173e77-92ec-4a87-a471-d6867837c180 2026-08-31 Warnings Exact identifier unii: TC2D6JAD40 unii: 362O9ITL9D EAYONYUMT NECK PAIN RELIEF MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a450e68-07a7-a4bb-e063-6294a90a97c9 2026-08-30 Warnings Exact identifier application number: M017 EAYONYUM BACK PAIN RELIEVING MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a458280-4f9c-5af6-e063-6394a90acb2e 2026-08-30 Warnings Exact identifier application number: M017 EAYONYUM KNEE PAIN RELIEVING MENTHOL Wuhan Ruihengjie Technology Co., Ltd. 5a45d19f-c753-71eb-e063-6294a90a4805 2026-08-30 Warnings Exact identifier application number: M017 Good Neighbor Pharmacy Hydrocortisone With Aloe for Sensitive Skin HYDROCORTISONE AmerisourceBergen c5c5b5ca-b4d4-4fa8-b647-b3ccb2966495 2026-08-30 Warnings Exact identifier application number: M017 Allergy Relief DIPHENHYDRAMINE HCL DOLGENCORP, LLC 69af44c2-390c-4223-889a-d5555aef5778 2026-08-28 Warnings Exact identifier unii: TC2D6JAD40 acetaminophen extra strength ACETAMINOPHEN Sam's West Inc dd99efd0-4ca4-4dc6-a940-bebd17ac8f8d 2026-08-28 Warnings Exact identifier application number: M013 rxcui: 198440 unii: 362O9ITL9D Wal Som Nighttime Sleep Aid Nighttime DIPHENHYDRAMINE HCL Walgreens 4cb0f9ab-1be1-4b41-a233-bbd0327036e2 2026-08-28 Warnings Exact identifier unii: TC2D6JAD40 Aspirin 81 mg ASPIRIN HAWAII REPACK, INC. ac94cce3-9a39-41de-bb8b-10a5e5b8e83b 2026-08-28 Warnings Exact identifier application number: M013 Olu Pain Management LIDOCAINE AND CAMPHOR HAWAII REPACK, INC. 31ed3d82-ba12-46b2-b0ec-7e5e019efc10 2026-08-28 Warnings Exact identifier application number: M017 4% Lidocaine Patches 4% LIDOCAINE PATCHES Shenzhen Chaoxiji Technology Co.,Ltd. 5a177987-7c05-f07f-e063-6394a90aa9ba 2026-08-28 Warnings Exact identifier application number: M017 Sodium Bicarbonate SODIUM BICARBONATE REMEDYREPACK INC. 96093b76-5d98-4d2b-b851-20207a8864db 2026-08-28 Warnings, Adverse reactions Exact identifier unii: 8MDF5V39QO Orajel 4X Medicated Toothache and Gum BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE Church & Dwight Co., Inc. 5a1b4133-0eac-2f8f-e063-6394a90af8f6 2026-08-28 Warnings Exact identifier unii: F5UM2KM3W7
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.