UZO Hand Sanitizer

Product NDC
79740-005
11-digit product format
797400005
Labeler code
79740
Product ID
79740-005_b1c099fb-64ee-c252-e053-2a95a90a8c11
Type
HUMAN OTC DRUG
Nonproprietary name
Hand Sanitizer
Dosage form
LIQUID
Route
TOPICAL
Labeler
ANTHOS GROUP, INC, THE
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct79740-005IInactivated by FDA2026-09-14
excluded packagepackage79740-00579740-005-01IInactivated by FDA2026-09-14

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 · 10 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage79740-005-01d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage79740-005-01f5e01cc5f278…a2eaf40c39c3…
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage79740-005-01fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage79740-005-0186f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage79740-005-01bd6a592717d7…303034d00443…

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79740-005-01UZO Hand Sanitizer240 mL in 1 BOTTLELIQUID2402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79740-005UZO HAND SANITIZER (HAND SANITIZER) LIQUID [ANTHOS GROUP, INC, THE]2Legacy NDC, 1 package rows20240221_b1c0a0d3-790a-3c04-e053-2995a90aadb4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
582753ethanol 70 % Topical SolutionPSNb1c0a0d3-790a-3c04-e053-2995a90aadb42
582753ethanol 0.7 ML/ML Topical SolutionSCDb1c0a0d3-790a-3c04-e053-2995a90aadb42
582753ethanol 70 % Topical SolutionSYb1c0a0d3-790a-3c04-e053-2995a90aadb42
582753ethyl alcohol 70 % Topical SolutionSYb1c0a0d3-790a-3c04-e053-2995a90aadb42

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79740-005-0179740000501240 mL in 1 BOTTLE (79740-005-01) 240 ml2020-03-300000-00-00NoNoCurrent