FDA.reportPublic FDA data

Foaming Hand Sanitizer

Product NDC
83986-118
11-digit product format
839860118
Labeler code
83986
Product ID
83986-118_5c26fadc-8cf0-669c-e063-6394a90aa52f
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
UpLift Brands LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-29
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

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 packagepackage83986-11883986-118-44DDiscontinued by firm2026-10-05

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 · 1 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage83986-11883986-118-44DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

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
Foaming Hand Sanitizer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.3 mg/mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-118-44Foaming Hand Sanitizer532 mL in 1 BOTTLE, PLASTICLIQUID5326
83986-118-45Foaming Hand Sanitizer1150 mL in 1 BOTTLE, PLASTICLIQUID11506
83986-118-86Foaming Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICLIQUID10006
83986-118-96Foaming Hand Sanitizer221 mL in 1 BOTTLE, PLASTICLIQUID2216

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83986-118FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [UPLIFT BRANDS LLC]4Current NDC, 4 package rows20250322_f8ca7e87-e5f1-4ef2-b389-02d318ccf78f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSNf8ca7e87-e5f1-4ef2-b389-02d318ccf78f6
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCDf8ca7e87-e5f1-4ef2-b389-02d318ccf78f6
1020365benzalkonium chloride 0.13 % Topical FoamSYf8ca7e87-e5f1-4ef2-b389-02d318ccf78f6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83986-118-4483986011844532 mL in 1 BOTTLE, PLASTIC532 mlHistorical
83986-118-45839860118451150 mL in 1 BOTTLE, PLASTIC (83986-118-45) 1150 ml2024-02-29NoNoCurrent
83986-118-86839860118861000 mL in 1 BOTTLE, PLASTIC (83986-118-86) 1000 ml2024-02-29NoNoCurrent
83986-118-9683986011896221 mL in 1 BOTTLE, PLASTIC (83986-118-96) 221 ml2024-02-29NoNoCurrent