Home NDC 58443-0648 NDC 58443-0648 - Panama Jack Burn Relief Gel with Lidocaine 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 58443-0648
Package NDCs from labels 58443-0648-4
Manufacturer Prime Enterprises Inc.
Effective date 2024-05-02
Current FDA listing Not matched in FDA.report NDC product tables
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 72 of 293 · 5,854 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Anti Bacterial Hand Gel Fiji White Sands ALCOHOL Bath & Body Works, Inc. 461420e0-a5b1-81df-e063-6394a90a94ec 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Anti Bacterial Hand Gel Winter ALCOHOL Bath & Body Works, Inc. 4613ce33-6881-e7c8-e063-6394a90a4090 2026-03-09 Warnings Exact identifier unii: 3K9958V90M Natouch Antifungal Antiseptic Wipes ANTIFUNGAL ANTISEPTIC WIPES Natouch LLC 4c84c556-8d0b-ec28-e063-6294a90af1d3 2026-03-08 Warnings Exact identifier unii: 3K9958V90M WowDay Medicated Hemorrhoidal Flushable Wipes MEDICATED HEMORRHOIDAL FLUSHABLE WIPES WowDay LLC 4c603b27-4835-bc40-e063-6394a90a8ea2 2026-03-06 Warnings Exact identifier unii: L7T10EIP3A Heal and Rescue Bunion Pain Relief LIDOCAINE HCL, MENTHOL Rooftop Consumer Health, Inc 4c60d4d3-e0a9-6f93-e063-6394a90a16af 2026-03-06 Warnings Exact identifier unii: L7T10EIP3A unii: V13007Z41A 2-Pack Facial Serum 2-PACK FACIAL SERUM Guangzhou Ariel Biotech Co., Ltd. 27c7f645-cfb3-6db1-e063-6394a90a42ff 2026-03-06 Warnings Exact identifier unii: 059QF0KO0R Muscle Meltdown External Analgesic Plaster MENTHOL, METHYL SALICYLATE Big 5 Nutrition LLC 0f0720fd-70d9-47f3-aebd-9d3f17379833 2026-03-06 Warnings Exact identifier unii: L7T10EIP3A JUST CBD - PAIN RELIEF MENTHOL, CAMPHOR Just Brands LLC 4c493c0b-c58e-cb56-e063-6394a90a9395 2026-03-05 Warnings Exact identifier unii: L7T10EIP3A SPA HAND SANITIZER WRTER MELON SPLASH ETHYL ALCOHOL Rejoice International Corp. 4c53620d-01ee-8ddd-e063-6294a90a8a2b 2026-03-05 Warnings Exact identifier unii: 3K9958V90M Smart Care PISTACHIO CREME HAND SANITIZER ETHYL ALCOHOL Ashtel Studios, Inc. e763a268-b8d0-4237-bf8e-28433c0e80b2 2026-03-05 Warnings Exact identifier unii: 3K9958V90M SSDC Gel Hand Sanitizer ALCOHOL Ecolab Inc. 56fd749e-67d2-4d6f-b681-c0a44db9eef3 2026-03-04 Warnings Exact identifier unii: 3K9958V90M CVS Foot Pain LIDOCAINE HYDROCHLORIDE CVS Pharmacy 4c3350c3-2e3e-093c-e063-6394a90a3475 2026-03-04 Warnings Exact identifier unii: V13007Z41A Game On Sport MENTHOL Natural Essentials, Inc 4c3411dc-5378-bd93-e063-6394a90a8406 2026-03-04 Warnings Exact identifier unii: L7T10EIP3A Hand Sanitizer ALCOHOL Trifecta Pharmaceuticals USA 0ba469a8-53f3-eb8e-e063-6294a90a1efc 2026-03-04 Warnings Exact identifier unii: 3K9958V90M Walgreens Unscented Pain Relieving LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL Walgreen Co. 41eadb4f-2ca5-42a1-e063-6294a90ab4e2 2026-03-04 Warnings Exact identifier unii: V13007Z41A Avant Foaming Hand Sanitizer ALCOHOL B4 Soap LLC 6cc57ff1-e49b-4c15-b997-886a29d3fe1c 2026-03-04 Warnings Exact identifier unii: 3K9958V90M Smart Care FRENCH VANILLA HAND SANITIZER ETHYL ALCOHOL Ashtel Studios Inc. 047f107b-c4d7-42d4-9c9c-5af8280be758 2026-03-04 Warnings Exact identifier unii: 3K9958V90M Everyone Hand Sanitizer Lavender Aloe ALCOHOL EO Products, LLC d15c1fb9-b25b-45b8-a119-ee4c86c8d91c 2026-03-03 Warnings Exact identifier unii: 3K9958V90M Advanced Hand Sanitizer ETHYL ALCOHOL Amazon.Com Services LLC 85421e9a-f1c9-4793-9479-8a072a610ed7 2026-03-03 Warnings, Adverse reactions Exact identifier unii: 3K9958V90M Sunburn Relief Gel LIDOCAINE HCL Amazon.com Services LLC adb638ec-4a7c-42f2-b249-0ac53a8dd4b2 2026-03-03 Warnings, Adverse reactions Exact identifier unii: V13007Z41A
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.