Home NDC 63645-174 Sanell Hand Sanitizer
Product NDC 63645-174
11-digit product format 636450174
Labeler code 63645
Product ID 63645-174_33dd4273-5402-5be0-e063-6394a90a41c1
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler OraLabs
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-08-12
Substance ALCOHOL
Active strength 6.3 mL/10mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 14 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 63645-174-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 63645-174-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 63645-174-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 63645-174-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 63645-174-02 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 63645-174-02 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 63645-174-02 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sanell Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 6.3 mL/10mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1798385 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63645-174-02 Sanell Hand Sanitizer 10 mL in 1 BOTTLE SPRAY 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63645-174 SANELL HAND SANITIZER (ALCOHOL) SPRAY [ORALABS] 3 Current NDC, Legacy NDC, 1 package rows 20250429_0a6cc2a8-f568-45ae-8d82-a70103c774c7.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 108 of 114 · 2,275 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Northside Hospital Amenity Kit--GI Dept ALCOHOL ASP Global, LLc c284eba4-0b92-4981-b3f8-d8d99b58bdfd 2024-01-10 Warnings Exact identifier application number: M003 Meijer 3 Hydrogen Peroxide Wipes HYDROGEN PEROXIDE Meijer, Inc. 33143d87-3e57-4a17-a96c-b699ad034b5b 2024-01-09 Warnings Exact identifier application number: M003 Meijer 70 Isopropyl Alcohol Wipes First Aid Antiseptic ISOPROPYL ALCOHOL Meijer, Inc 2046162f-cb70-416c-ae37-14999883a807 2024-01-09 Warnings Exact identifier application number: M003 Lightning X Antiseptic BENZALKONIUM CHLORIDE Nantong Health & Beyond Hygienic Products Inc. 0e6b10e7-6e84-6bfc-e063-6294a90a8537 2024-01-08 Warnings Exact identifier application number: M003 Hydrogen Peroxide HYDROGEN PEROXIDE 3.0% Trifecta Pharmaceuticals USA, LLC. e4e45f11-7cd4-e693-e053-2a95a90a4c34 2024-01-02 Warnings Exact identifier application number: M003 GLOBAL CARE GOLD ANTIBACTERIAL HAND BENZALKONIUM CHLORIDE NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. 27ba0f30-e066-f240-e063-6394a90ae7cb 2024-01-01 Warnings Exact identifier application number: M003 Freskaro Decolorized Iodine ALCOHOL Pharma Nobis, LLC fbd222a2-1151-99b9-e053-6394a90a8bb8 2023-12-28 Warnings Exact identifier application number: M003 Alcohol Prep ISOPROPYL ALCOHOL Topco Associates 65270825-48b1-49e7-a14e-f73df9beb9dd 2023-12-27 Warnings Exact identifier application number: M003 Humco Hydrogen Peroxide HYDROGEN PEROXIDE 3% Pharma Nobis, LLC e42f876d-0477-c4d5-e053-2a95a90ae6d4 2023-12-26 Warnings Exact identifier application number: M003 Ethyl Rubbing Alcohol 70 Percent ETHYL ALCOHOL Pharma Nobis, LLC e42fccc2-1b50-e7f3-e053-2a95a90aef39 2023-12-26 Warnings Exact identifier application number: M003 Isopropyl Alcohol 70 Percent With Wintergreen Oil ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f6c6d-c4e1-02c6-e053-2995a90a3ace 2023-12-26 Warnings Exact identifier application number: M003 CVS Merthiolate BENZALKONIUM CHLORIDE CVS Pharmacy dd498ab1-8350-41aa-86fc-2db57005f3e2 2023-12-22 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE IODINE 10% Pharma Nobis, LLC e42eee1b-3539-fb17-e053-2995a90af61d 2023-12-22 Warnings Exact identifier application number: M003 Decolorized Iodine ETHYL ALCOHOL Pharma Nobis, LLC e21dd43b-3712-cb16-e053-2a95a90ac276 2023-12-22 Warnings Exact identifier application number: M003 Isopropyl Rubbing Alcohol 70 Percent ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f727c-beb0-fe9d-e053-2995a90aafea 2023-12-22 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE IODINE GARGLE 0.5% Pharma Nobis, LLC e42ee827-b350-7b56-e053-2a95a90a69cf 2023-12-22 Warnings Exact identifier application number: M003 Merthiolate BENZALKONIUM CHLORIDE Pharma Nobis, LLC e42f727c-beaf-fe9d-e053-2995a90aafea 2023-12-22 Warnings Exact identifier application number: M003 Isopropyl Alcohol 91 Percent ISOPROPYL ALCOHOL Pharma Nobis, LLC e42f6c6d-c4e0-02c6-e053-2995a90a3ace 2023-12-22 Warnings Exact identifier application number: M003 RevitaDERM Wound Care BENZALKONIUM CHLORIDE Blaine Labs Inc. 9254dada-4e32-43a0-892b-c488d68e23e7 2023-12-21 Warnings Exact identifier application number: M003 NUMSTAT Antiseptic and Pain Relieving Prep Pad ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD Spectra Medical Devices, LLC 07d20040-9dd9-0aba-e063-6294a90ab7cf 2023-12-20 Warnings Exact identifier application number: M003
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63645-174-02 63645017402 10 mL in 1 BOTTLE (63645-174-02) 10 ml 2019-08-12 0000-00-00 No No Current