Home NDC 75742-022 Hand sanitizer 2oz 2pk with aloe vera
Product NDC 75742-022
11-digit product format 757420022
Labeler code 75742
Product ID 75742-022_47afd8f9-9abf-f8ff-e063-6394a90aff33
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol 70%
Dosage form GEL
Route TOPICAL
Labeler Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-10
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 · 27 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 75742-022-02 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 75742-022-01 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 75742-022-02 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 75742-022-01 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 75742-022-02 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 75742-022-01 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 75742-022-02 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 75742-022-01 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 75742-022-02 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 75742-022-01 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 75742-022-02 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 75742-022-01 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 75742-022-01 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 75742-022-02 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 75742-022-01 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 75742-022-02 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 75742-022-01 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 75742-022-02 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 Hand sanitizer 2oz 2pk with aloe vera
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
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 581662 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 75742-022-01 Hand sanitizer 2oz 2pk with aloe vera 59 mL in 1 BOTTLE GEL 59 2 75742-022-02 Hand sanitizer 2oz 2pk with aloe vera 59 mL in 1 BOTTLE GEL 59 2 75742-022-02 Hand sanitizer 2oz 2pk with aloe vera 2 in 1 BOX GEL 2 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 75742-022 HAND SANITIZER 2OZ 2PK WITH ALOE VERA (ETHYL ALCOHOL 70%) GEL [ZHEJIANG GUOYAO JINGYUE AEROSOL CO., LTD.] 1 Current NDC, 3 package rows 20230911_04fe378d-ee1e-ad52-e063-6294a90ae146.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 100 of 114 · 2,270 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Target Up and Up 2-in-1 Hand Sanitizer BENZETHONIUM CHLORIDE TARGET CORPORATION e069c9e6-024d-5482-e053-2995a90a767d 2024-10-14 Warnings Exact identifier application number: M003 Meridian Wrapped antibacterial Deodorant BENZETHONIUM CHLORIDE Bob Barker Company Inc. 7c834c1d-7930-4909-a600-6de9698e2b17 2024-10-14 Warnings Exact identifier application number: M003 Meridian Unwrapped antibacterial Deodorant BENZETHONIUM CHLORIDE Bob Barker Company Inc. adc10d22-a913-4bfa-a3f7-d6d5778f07ca 2024-10-14 Warnings Exact identifier application number: M003 First Aid Antiseptic Pain Relieving BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE Hubei Changjian Medical Products Co., Ltd. 9cb3759a-35d9-4f6b-94ad-fafd4bc600bd 2024-10-11 Warnings Exact identifier application number: M003 Antiseptic Towelette BENZALKONIUM CHLORIDE Hubei Changjian Medical Products Co., Ltd. bf045881-9636-4000-a0ac-f6aab6b81832 2024-10-11 Warnings Exact identifier application number: M003 Antiseptic Povidone-lodine Prep Pad POVIDONE-IODINE Hubei Changjian Medical Products Co., Ltd. 2cacf2e0-0192-4e0f-88a6-e3eee3af5471 2024-10-11 Warnings Exact identifier application number: M003 Antiseptic ETHANOL McKesson 6637290d-6ae4-5a83-e053-2991aa0a81c6 2024-10-11 Warnings Exact identifier application number: M003 Antibacterial BENZETHONIUM CHLORIDE McKesson 58892abf-e0b9-83d9-e053-2a91aa0ad035 2024-10-11 Warnings Exact identifier application number: M003 Antibacterial BENZETHONIUM CHLORIDE McKesson 588a89cd-9481-6163-e053-2991aa0a9e3d 2024-10-11 Warnings Exact identifier application number: M003 McKesson Obstetrical Antiseptic Towelette BENZALKONIUM CHLORIDE McKesson Medical-Surgical 51a3dabe-25d3-47fd-b640-83e68f7e06de 2024-10-11 Warnings Exact identifier application number: M003 McKesson Benzalkonium Chloride Towelette BENZALKONIUM CHLORIDE McKesson Medical-Surgical cea36a9e-aac3-4494-a713-1dc64272d99c 2024-10-11 Warnings Exact identifier application number: M003 Alcohol Disinfecting Wipe ALCOHOL McKesson Medical-Surgical 64a0063d-a5da-4a46-9dca-16e4dbdac85c 2024-10-11 Warnings Exact identifier application number: M003 Mckesson Hand Cleanse and Soothe with Aloe CHLOROXYLENOL Mckesson Medical-Surgical Inc. 075cd889-948a-49dd-8927-e22f7a5bff99 2024-10-10 Warnings Exact identifier application number: M003 Hand Sanitizer HAND SANITIZER UNSCENTED CASAD Company, Inc 07a891a3-dcf7-438f-bbf7-a20b2aa7d7d7 2024-10-09 Warnings Exact identifier application number: M003 Hand Sanitizer HAND SANITIZER UNSCENTED CASAD Company, Inc 0933de73-94b1-448e-b39f-ecffabf95288 2024-10-09 Warnings Exact identifier application number: M003 EVERSOFT FOAMING HAND ANTI-BACTERIAL CHLOROXYLENOL Draco Hygienic Products Inc. e9d4767b-21f2-b68f-e053-2995a90a5aba 2024-10-08 Warnings Exact identifier application number: M003 FOAMING HAND ALCOHOL FOAM ALCOHOL Draco Hygienic Products Inc. 14860a19-e1e8-71fc-e063-6394a90a9df8 2024-10-08 Warnings Exact identifier application number: M003 FOAMING HAND ANTIBACTERIAL CHLOROXYLENOL Draco Hygienic Products Inc. 15256355-29ef-9b24-e063-6294a90a907d 2024-10-08 Warnings Exact identifier application number: M003 Germ Attack Hand Sanitizer ALCOHOL Natural Essentials, Inc. 4d156264-566d-4516-876c-b6f5823a97f5 2024-10-04 Warnings Exact identifier application number: M003 Germ Attack Hand Sanitizer ALCOHOL Natural Essentials, Inc. 9d3a4dfe-f31d-4def-bfc2-ece69d13f8e4 2024-10-04 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 Sample Exclude flag Status 75742-022-01 75742002201 59 mL in 1 BOTTLE (75742-022-01) 59 ml 2023-09-10 No No Current 75742-022-02 75742002202 2 BOTTLE in 1 BOX (75742-022-02) / 59 mL in 1 BOTTLE 2 bottle 2023-09-10 No No Current