Home NDC 44224-1000 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID
Product NDC 44224-1000
11-digit product format 442241000
Labeler code 44224
Product ID 44224-1000_42d68a3b-5d81-41cc-8de8-f14402850ff7
Type HUMAN OTC DRUG
Nonproprietary name BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL
Dosage form KIT
Labeler Tender Corp dba Adventure Medical Kits
Application part348
Marketing category OTC MONOGRAPH FINAL
Marketing start 2010-08-25
Marketing end 0000-00-00
Active strength 0
NDC exclude flag E
Listing certified through 2018-12-31
Current FDA listing Historical FDA.report record 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 · 44 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 44224-1000-1 I Inactivated by FDA d630ba8d3edf…732f749b63fb…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 44224-1000-1 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 44224-1000-1 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 44224-1000-1 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 44224-1000-1 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 44224-1000-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 44224-1000-1 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 44224-1000-1 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 44224-1000-1 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 44224-1000-1 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 44224-1000-1 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 44224-1000-1 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 44224-1000-1 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 44224-1000-1 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 44224-1000-1 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 44224-1000-1 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 44224-1000-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 44224-1000-1 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 44224-1000-1 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 44224-1000-1 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 44224-1000-1 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 44224-1000-1 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44224-1000-1 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID 1 in 1 KIT KIT 1 10 52124-0001-1 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID 0.8 mL in 1 PACKAGE SWAB 4.8 mL 0.4 mL in 100mL 10 52124-0008-1 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID 0.5 mL in 1 PACKAGE SWAB 0.5 mL 60 mL in 100mL 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 BENZALKONIUM CHLORIDE ACTIVE INGREDIENT F5UM2KM3W7 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 BENZOCAINE ACTIVE INGREDIENT U3RSY48JW5 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 ALCOHOL ACTIVE MOIETY 3K9958V90M ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 BENZALKONIUM ACTIVE MOIETY 7N6JUD5X6Y ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 BENZOCAINE ACTIVE MOIETY U3RSY48JW5 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 WATER INACTIVE INGREDIENT 059QF0KO0R ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44224-1000 ADVENTURE MEDICAL KITS 1 PERSON FIRST AID (BENZALKONIUM CHLORIDE, BENZOCAINE, SD ALCOHOL) KIT [TENDER CORP DBA ADVENTURE MEDICAL KITS] 10 Legacy NDC, 3 package rows 20101027_aab9d522-6c5c-4976-a718-76b14f4899bb.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 44224-1000-1 44224100001 1 in 1 KIT Historical 52124-0001-1 52124000101 0.8 mL in 1 PACKAGE 0.8 ml Historical 52124-0008-1 52124000801 0.5 mL in 1 PACKAGE 0.5 ml Historical