Home NDC 49314-0001 First Aid Antispetic
Product NDC 49314-0001
11-digit product format 493140001
Labeler code 49314
Product ID 49314-0001_3fe7ba5b-5fc3-c1b7-e063-6394a90a5b15
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SPRAY
Route TOPICAL
Labeler Unishield
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-20
Substance BENZALKONIUM CHLORIDE
Active strength .13 mg/mL
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 · 16 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 2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 49314-0001-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…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 49314-0001-1 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 49314-0001-1 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 49314-0001-1 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 49314-0001-1 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 49314-0001-1 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 49314-0001-1 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 49314-0001-1 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 First Aid Antispetic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49314-0001-1 First Aid Antispetic 59.1 mL in 1 BOTTLE, SPRAY SPRAY 59.1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49314-0001 FIRST AID ANTISPETIC (BENZALKONIUM CHLORIDE) SPRAY [UNISHIELD] 1 Current NDC, 1 package rows 20230320_f72851ba-bbdd-5533-e053-6294a90a8216.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 24 of 49 · 969 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join BBlove ALCOHOL WIPES BBLOVE ALCOHOL WIPES Shenzhen Shierjie Biological Engineering Co., LTD 1a451616-b16e-8aa7-e063-6294a90a26a1 2026-01-07 Warnings Exact identifier application number: M005 Wet wipes WET WIPES Shenzhen Shierjie Biological Engineering Co., LTD 273b3ae2-6dec-31a4-e063-6294a90aca89 2026-01-07 Warnings Exact identifier application number: M005 Bee Venom Fungal Nail Treatment Liquid BEE VENOM FUNGAL NAIL TREATMENT Shenzhen Earth Surface Trading Co., Ltd. 47c37468-ba5c-0d11-e063-6294a90ac554 2026-01-06 Warnings Exact identifier application number: M005 ProBliva Anti Fungal Shampoo. ANTIFUNGAL CAVTECH HOLDING LLC 47af9ff8-5d5c-4524-e063-6394a90ac91f 2026-01-05 Warnings Exact identifier application number: M005 Beauty Creations Pink Halo Hand Sanitizer Mist ETHYL ALCOHOL Nantong Health & Beyond Hygienic Products Inc. dda9f4cb-e431-4164-be61-0daf1a86d10f 2026-01-04 Warnings Exact identifier application number: M005 FUNGAL NAIL PATCHES UNDECYLENIC ACID Guangzhou Hechuang Commercial Service Co.,Ltd. 477c971d-829f-5040-e063-6394a90a41e4 2026-01-03 Warnings Exact identifier application number: M005 Nail Renovar Plus TOLNAFTATE SOHM, Inc 2c09925c-e63e-4d9b-8d76-b06bd2cba26c 2026-01-02 Warnings Exact identifier application number: M005 Natural Sense Full Body Cleansing Towel CLEANSING TOWEL Dr. Natural LLC 4742eec4-b7a3-2c89-e063-6294a90a19fc 2025-12-31 Warnings Exact identifier application number: M005 Lasolex AG MICONAZOLE NITRATE Puretek Corporation 4411142f-a8ec-c8c2-e063-6394a90aa25c 2025-12-31 Warnings Exact identifier application number: M005 Hermon Antifungal Stick 1% CLOTRIMAZOLE Beautivity LLC 474a5783-4488-034e-e063-6294a90a5de3 2025-12-31 Warnings Exact identifier application number: M005 SnugZ Hand Sanitizing Wipes HAND SANITIZING WIPES SnugZ/USA, LLC c5d9122a-2c67-2387-e053-2a95a90a2c3a 2025-12-29 Warnings Exact identifier application number: M005 Clotrimazole (Topical Solution), 1% CLOTRIMAZOLE Puro Pharma Inc. cb424fa8-3ed5-45cd-b03f-64675584b34e 2025-12-27 Warnings Exact identifier application number: M005 CLOTRIMAZOLE CLOTRIMAZOLE GRAXCELL PHARMACEUTICAL, LLC. 5f8ca6ad-cb25-1abf-e053-2a91aa0aca99 2025-12-25 Warnings Exact identifier application number: M005 CuraNails Antifungal Pen UNDECYLENIC ACID 25% Quality Discount Inc. 3e641d36-72f6-4682-bd31-f7cd04d857f2 2025-12-25 Warnings Exact identifier application number: M005 Opti-Nail 2-in-1 TOLNAFTATE Kramer Laboratories bc8a5492-8bd0-4c80-a270-e4958aeb5ed6 2025-12-23 Warnings Exact identifier application number: M005 ProBliva Medicated Anti Fungal ANTIFUNGAL CAVTECH HOLDING LLC 46852aea-028c-71c2-e063-6394a90a8055 2025-12-22 Warnings Exact identifier application number: M005 Terthon Clotrimazole 1% Antifungal Cream CLOTRIMAZOLE 1% SOLALIA LLC 468f1b1b-f67d-8b98-e063-6294a90a7f45 2025-12-22 Warnings Exact identifier application number: M005 Clotrimazole CLOTRIMAZOLE Granules USA, Inc. 6e63e29a-eb50-1790-e053-2a91aa0a3616 2025-12-22 Warnings Exact identifier application number: M005 TopCare Antifungal Maximum Strength UNDECYLENIC ACID TOPCO ASSOCIATES LLC 7c44fb4e-0eef-4ced-b03f-a02ebe6c0264 2025-12-22 Warnings Exact identifier application number: M005 Fungi Nail Toe and Foot TOLNAFTATE Kramer Laboratories a3ae043b-dc97-449b-b099-70bdf8e92482 2025-12-19 Warnings Exact identifier application number: M005
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 49314-0001-1 49314000101 59.1 mL in 1 BOTTLE, SPRAY (49314-0001-1) 59.1 ml 2023-03-20 No No Current