HAND SANITIZER

Product NDC
79805-001
Requested package NDC
79805-001-08
11-digit product format
798050001
Labeler code
79805
Product ID
79805-001_b54ddc53-47d9-809e-e053-2995a90af47a
Type
HUMAN OTC DRUG
Nonproprietary name
HAND SANITIZER
Dosage form
GEL
Route
TOPICAL
Labeler
JUXIN (Jiangsu) New Material Packaging Co., Ltd.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-03-30
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
68 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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage79805-00179805-001-08IInactivated by FDA2026-10-05

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 · 5 matching rows.

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

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2024-11-09 02:27 UTC · source 2024-11-08DDiscontinued by firmad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03DDiscontinued by firm367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09DDiscontinued by firm557ba5c1ecfa…9c80585c8c6e…
2022-04-09 23:13 UTC · source 2022-04-08IInactivated by FDA86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01IInactivated by FDAbd6a592717d7…303034d00443…

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 NDCProductDescriptionFormQuantityStrengthSPL version
79805-001-01HAND SANITIZER60 mL in 1 BOTTLEGEL605
79805-001-02HAND SANITIZER120 mL in 1 BOTTLEGEL1205
79805-001-03HAND SANITIZER300 mL in 1 BOTTLEGEL3005
79805-001-04HAND SANITIZER500 mL in 1 BOTTLEGEL5005
79805-001-05HAND SANITIZER3800 mL in 1 BOTTLEGEL38005
79805-001-06HAND SANITIZER90 mL in 1 BOTTLEGEL905
79805-001-07HAND SANITIZER100 mL in 1 BOTTLEGEL1005
79805-001-08HAND SANITIZER750 mL in 1 BOTTLEGEL7505
79805-001-09HAND SANITIZER1000 mL in 1 BOTTLEGEL10005
79805-001-10HAND SANITIZER18 mL in 1 BOTTLEGEL185
79805-001-11HAND SANITIZER250 mL in 1 BOTTLEGEL2505
79805-001-12HAND SANITIZER2000 mL in 1 BOTTLEGEL20005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79805-001HAND SANITIZER GEL [JUXIN (JIANGSU) NEW MATERIAL PACKAGING CO., LTD.]5Legacy NDC, 12 package rows20250105_ab2878a9-5f9c-79ec-e053-2995a90adf97.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1037039ethanol 68 % Topical GelPSNab2878a9-5f9c-79ec-e053-2995a90adf975
1037039ethanol 0.68 ML/ML Topical GelSCDab2878a9-5f9c-79ec-e053-2995a90adf975
1037039ethanol 68 % Topical GelSYab2878a9-5f9c-79ec-e053-2995a90adf975

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79805-001-0879805000108750 mL in 1 BOTTLE (79805-001-08) 750 ml2020-03-300000-00-00NoNoCurrent