Home NDC 61333-222-01 NDC 61333-222-01 - LIGHTS Antiseptic and Pain Relieving Prep Pad 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 61333-222
Requested NDC 61333-222-01
Package NDCs from labels 61333-222-01, 61333-222-02
Manufacturer Lights Medical Manufacture Co., Ltd.
Effective date 2026-08-07
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 78 of 265 · 5,292 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join GRANULOTION Hemorrhoidal MENTHOL, ZINC OXIDE GL Health, Inc. 1a32741c-5e4a-40e5-b15a-8233c5bdb92b 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A VAPORX CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL AKRON PHARMA INC 51b32162-0c5a-4b5b-999a-34337d816603 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A Equate Orasol 20% BENZOCAINE WAL-MART STORES INC. 08404780-8252-4484-b1c3-8970803f74f8 2026-01-19 Warnings Exact identifier unii: U3RSY48JW5 Scent Theory Hand Sanitizers Coastal Mist, Boardwalk Treats, Firecracker Freeze ALCOHOL Scent Theory Products LLC 48c3d5e9-2d57-5a46-e063-6394a90a0722 2026-01-19 Warnings Exact identifier application number: M003 AsperFlex MENTHOL AND METHYL SALICYLATE Akron Pharma Inc. 117de175-976d-44f3-85ed-3d127fbe3a7c 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A Equate Pain Relieving Ultra Strength CAMPHOR, MENTHOL, METHYL SALICYLATE Wal-Mart Stores Inc 5ed1d7b3-925e-4a18-8e15-636f5b442ad7 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A Hydroseptine ZINC OXIDE, MENTHOL AKRON PHARMA INC 5359d92e-641e-4076-9d91-18daee58a30e 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A Equate Medicated Pain Relieving Patch, Large 6-Count CAMPHOR, MENTHOL, METHYL SALICYLATE Walmart Stores Inc 2c25cd7a-7e7b-5add-e063-6294a90a9e9b 2026-01-19 Warnings Exact identifier unii: L7T10EIP3A HealthWise Chest Rub CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL Veridian Healthcare ce3ceffd-3ff5-3795-e053-2995a90a827f 2026-01-18 Warnings Exact identifier unii: L7T10EIP3A Neuropathy Pain Relief Cream MENTHOL CREAM Owell Naturals Brand, LLC 48979093-2992-5fd8-e063-6394a90a815d 2026-01-17 Warnings Exact identifier unii: L7T10EIP3A hi peach layne ETHYL ALCOHOL Zhejiang Jinghui Cosmetics Share Co., Ltd. 487b648a-1680-6de5-e063-6394a90ab852 2026-01-16 Warnings Exact identifier application number: M003 hi peach layne ETHYL ALCOHOL Zhejiang Jinghui Cosmetics Share Co., Ltd. 487e6851-1ca3-f9db-e063-6394a90a56f1 2026-01-16 Warnings Exact identifier application number: M003 CVS Cherry Cough Drops MENTHOL CVS Pharmacy de5c4b94-0420-5d43-e053-2995a90aa5a5 2026-01-16 Warnings Exact identifier unii: L7T10EIP3A CVS Honey Lemon Cough Drops MENTHOL CVS Pharmacy de963dc3-8108-440f-e053-2995a90a906f 2026-01-16 Warnings Exact identifier unii: L7T10EIP3A CVS SF Menthol Cough Drops MENTHOL CVS Pharmacy e08f8ca3-b683-4964-e053-2a95a90afabb 2026-01-16 Warnings Exact identifier unii: L7T10EIP3A CVS SF Honey Lemon Cough Drops MENTHOL CVS Pharmacy e0cdeccf-c32f-318a-e053-2a95a90ac401 2026-01-16 Warnings Exact identifier unii: L7T10EIP3A Mixed Berry Throat and Cough Lozenges BENZOCAINE CVS Pharmacy 737b1c88-1a44-68cf-e053-2991aa0a35b6 2026-01-16 Warnings Exact identifier unii: U3RSY48JW5 Instant Hand Sanitizer ALCOHOL Safetec of America, Inc. c3f0556d-f967-4f19-922c-57a2bf184892 2026-01-16 Warnings Exact identifier application number: M003 Instant Hand Sanitizer ALCOHOL Safetec of America 3b5b46d0-308a-4649-8384-246da3a18ba1 2026-01-16 Warnings Exact identifier application number: M003 Instant Hand Sanitizer ALCOHOL Safetec of America bf69cc74-ebe9-40c3-a95a-a489492cc693 2026-01-16 Warnings Exact identifier application number: M003
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.