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 114 of 264 · 5,267 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dragon Pain Relieving Balm CAMPHOR, MENTHOL Americanna Wellness, Inc. 002db658-6b1f-ea49-e063-6294a90ae3e7 2025-11-24 Warnings Exact identifier unii: L7T10EIP3A Dragon Pain Relieving Balm CAMPHOR, MENTHOL Americanna Wellness, Inc. 002997d0-3176-3918-e063-6294a90a4408 2025-11-24 Warnings Exact identifier unii: L7T10EIP3A Dragon Pain Relieving CAMPHOR, MENTHOL AMERICANNA WELLNESS, INC. 0d1059cc-1b0b-4e7b-e063-6294a90a56ea 2025-11-24 Warnings Exact identifier unii: L7T10EIP3A GuruNanda Pain Relief MENTHOL AND CAMPHOR GURUNANDA, LLC 3ca78342-cc6d-5f6b-e063-6294a90a3f1c 2025-11-24 Warnings Exact identifier unii: L7T10EIP3A Dragon Pain Relieving CAMPHOR, MENTHOL AMERICANNA WELLNESS, INC. 0d118256-90ee-28ef-e063-6394a90a21e8 2025-11-24 Warnings Exact identifier unii: L7T10EIP3A Lights Swabsticks ISOPROPYL ALCOHOL Lights Medical Manufacture Co., Ltd. 4435a4e6-46ae-f49b-e063-6394a90a1d9e 2025-11-22 Warnings Exact identifier application number: M003 unii: ND2M416302 FloraMedis Hand Sanitizer HAND SANITIZER Sichuan Pengtai Qifan Technology Co., Ltd 4415ca9f-10b1-88f7-e063-6294a90a2e09 2025-11-21 Warnings Exact identifier application number: M003 DG 4x Medicated Tooth and Gum Cream BENZOCAINE Dollar General b2c156f0-6d11-1eba-e053-2995a90a6db8 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 unii: L7T10EIP3A 4x Medicated Toothache and Gum Gel BENZOCAINE CVS a7577d5f-69cf-3f32-e053-2995a90aaba5 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 unii: L7T10EIP3A Rite Aid Professional Strength BENZOCAINE Rite Aid 31ce0cb3-a43a-41bd-b030-21f91f2b1368 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Rite Aid Maximum Strength BENZOCAINE Rite Aid 5e216587-5384-464a-a4dd-07943668cabd 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 NBE Anbesol BENZOCAINE Walgreens dd2a3125-32f8-5fff-e053-2995a90ac720 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Walgreens Maximum Strength BENZOCAINE Walgreens 2ef0eb2c-b614-44e2-b9b3-97b02c654977 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 Toothache and Gum Relief Cushions BENZOCAINE Rite Aid 9970d485-0b78-1438-e053-2995a90ad32c 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 unii: L7T10EIP3A Nighttime 4X Medicated Cream BENZOCAINE Rite Aid 21645ed1-2dc0-223a-e063-6394a90ab021 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 unii: L7T10EIP3A 4x Medicated Gum Cream BENZOCAINE Albertsons b81a308c-9c30-0e3d-e053-2a95a90a15d2 2025-11-21 Warnings Exact identifier unii: U3RSY48JW5 unii: L7T10EIP3A MENTHOL, CAMPHOR MENTHOL, CAMPHOR SUNSET NOVELTIES, INC b0edd9d9-951f-d3dd-e053-2995a90a8d5a 2025-11-21 Warnings Exact identifier unii: L7T10EIP3A Throat Coat Eucalyptus Mint MENTHOL Traditional Medicinals, Inc. a7a86f1b-30e8-6f5d-e053-2a95a90a2a82 2025-11-21 Warnings Exact identifier unii: L7T10EIP3A Throat Coat Sweet Orange Fennel MENTHOL Traditional Medicinals, Inc. 4538248f-11cc-d6b2-e063-6294a90a652c 2025-11-21 Warnings Exact identifier unii: L7T10EIP3A Eyewash Additive Concentrate WATER AND PROPYLENE GLYCOL Haws Corporation dd168403-398c-41ff-b1df-d93e4ff39de3 2025-11-20 Warnings Exact identifier unii: 059QF0KO0R
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.