Home NDC 48256-0002-01 NDC 48256-0002-01 - WHITE FLOWER ANALGESIC BALM 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 48256-0002
Requested NDC 48256-0002-01
Package NDCs from labels 48256-0002-1, 48256-0002-2, 48256-0002-4, 48256-0002-3, 48256-0002-01
Manufacturer HOE HIN PAK FAH YEOW MANUFACTORY LTD | HOE HIN PAK FAH YEOW MFY LTD
Effective date 2025-10-21
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type DRUG FACTS HOE HIN PAK FAH YEOW MANUFACTORY LTD | HOE HIN PAK FAH YEOW MFY LTD 2025-10-21 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48256-0002-1 WHITE FLOWER ANALGESIC BALM 20 mL in 1 BOTTLE, GLASS OIL 20 9 48256-0002-2 WHITE FLOWER ANALGESIC BALM 10 mL in 1 BOTTLE, GLASS OIL 10 9 48256-0002-3 WHITE FLOWER ANALGESIC BALM 5 mL in 1 BOTTLE, GLASS OIL 5 9 48256-0002-4 WHITE FLOWER ANALGESIC BALM 2.5 mL in 1 BOTTLE, GLASS OIL 2.5 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48256-0002 WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 8 Current NDC, Legacy NDC, 4 package rows 20231003_f3e3b8b5-b12b-49ac-9318-b0c358b136e9.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAMPHOR (SYNTHETIC) ACTIVE INGREDIENT 5TJD82A1ET WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 MENTHOL ACTIVE INGREDIENT L7T10EIP3A WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 METHYL SALICYLATE ACTIVE INGREDIENT LAV5U5022Y WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 CAMPHOR (SYNTHETIC) ACTIVE MOIETY 5TJD82A1ET WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 MENTHOL ACTIVE MOIETY L7T10EIP3A WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 EUCALYPTUS OIL INACTIVE INGREDIENT 2R04ONI662 WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 LAVENDER OIL INACTIVE INGREDIENT ZBP1YXW0H8 WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4 PEPPERMINT OIL INACTIVE INGREDIENT AV092KU4JH WHITE FLOWER ANALGESIC BALM (CAMPHOR, MENTHOL AND METHYL SALICYLATE) OIL [HOE HIN PAK FAH YEOW MANUFACTORY LTD] 4
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 61 of 201 · 4,009 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join 4x Medicated Toothache and Gum Cream BENZOCAINE HEB a71c5259-cbcf-7566-e053-2995a90a2cb6 2026-01-08 Warnings Exact identifier unii: L7T10EIP3A 3x Medicated Mouth Sore Gel BENZOCAINE HEB a71c5259-cbd1-7566-e053-2995a90a2cb6 2026-01-08 Warnings Exact identifier unii: L7T10EIP3A 4x Medicated Toothache and Gum Gel BENZOCAINE Publix Super Markets INC 16eb9d15-dba3-36e6-e063-6394a90ab859 2026-01-08 Warnings Exact identifier unii: L7T10EIP3A Toothache and Gum Relief BENZOCAINE, MENTHOL CVS Pharmacy 814ec7bf-f825-1095-e053-2a91aa0aee59 2026-01-08 Warnings Exact identifier unii: L7T10EIP3A DZUL ARTHRITIS PAIN RELIEF MENTHOL Caball Sales, Inc. 159c301c-d462-bb2c-e063-6394a90a9e5a 2026-01-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A DZUL - LIDO CREME LIDOCAINE HCL, MENTHOL Caball Sales, Inc. 063387e4-a1b1-a467-e063-6294a90a6cbd 2026-01-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A TOPICAINE LIDOCAINE 4% ESBA LABORATORIES INC. 7f96e980-891e-743d-e053-2a91aa0aea5f 2026-01-08 Warnings Exact identifier application number: M017 LUBRICAINE LIDOCAINE 4% ESBA LABORATORIES INC. 9d7416b1-607d-34e0-e053-2a95a90aa3c3 2026-01-08 Warnings Exact identifier application number: M017 0.5% LIDOCAINE BURN RELIEF LIDOCAINE HYDROCHLORIDE Universal Distribution Center LLC 0a1aeff0-bade-457b-a0ac-099d646c0b2e 2026-01-08 Warnings Exact identifier application number: M017 4% MENTHOL COLD THERAPY MENTHOL Universal Distribution Center LLC 66892993-a755-4584-b2a8-2e8d7ac70593 2026-01-08 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Private Label Antifungal Barrier Cream 2% MICONAZOLE NITRATE CREAM Swiss-American CDMO, LLC e74bddea-c1ac-4e4e-84bd-5a9defb85b2d 2026-01-08 Warnings Exact identifier application number: M017 2.0% LIDOCAINE BURN LIDOCAINE HYDROCHLORIDE Universal Distribution Center LLC e1911279-85f7-4053-b6da-8f4e991347a2 2026-01-08 Warnings Exact identifier application number: M017 Lidocaine Pain Relief Patch LIDOCAINE PAIN RELIEF PATCH Henan Shouerkang Health Industry Co., Ltd 29aefb41-bf5b-1c3c-e063-6294a90a9570 2026-01-07 Warnings Exact identifier unii: L7T10EIP3A POMG PAIN RELIEF ROLLER LIDOCAINE HYDROCHLORIDE, MENTHOL POMG LLC 1fa980fb-fc0e-fdd0-e063-6394a90adc13 2026-01-07 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Artridon Glucosamine MENTHOL, METHYL SALICYLATE Pharmadel LLC 73572156-4cce-0669-e053-2991aa0aaecc 2026-01-07 Warnings Exact identifier application number: M017 unii: L7T10EIP3A unii: LAV5U5022Y HealthWise Cooling Pain Relief MENTHOL Veridian Healthcare 6e2ad0ab-e3a8-4e3a-8f1d-2cd6351185bd 2026-01-07 Warnings Exact identifier application number: M017 unii: L7T10EIP3A Hydrocortisone 1% Anti-Itch Cream HYDROCORTISONE DLC Laboratories, Inc. 16eeec2c-065d-4da0-e063-6294a90a3873 2026-01-07 Warnings Exact identifier application number: M017 Maximum Strength Hydrocortisone HYDROCORTISONE DLC Laboratories, Inc caf50f12-f35c-4e9e-8ef7-3b0c84e225ee 2026-01-07 Warnings Exact identifier application number: M017 EARTHS CARE MUSCLE AND JOINT RUB CAMPHOR DLC Laboratories, Inc. 71e33e06-4dc3-4ead-a122-ff89d93a64de 2026-01-07 Warnings Exact identifier application number: M017 VAPOREX CAMPHOR (SYNTHETIC), EUCALYPTUS OIL, AND MENTHOL DLC Laboratories, Inc. 971943b1-4199-4f75-9d2d-61242d346b5f 2026-01-07 Warnings Exact identifier unii: L7T10EIP3A unii: 5TJD82A1ET unii: 2R04ONI662
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.