Foaming Hand Sanitizer

Product NDC
83986-118
Requested package NDC
83986-118-45
11-digit product format
839860118
Labeler code
83986
Product ID
83986-118_4cc3d5ce-f601-93a5-e063-6294a90a7296
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

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1020365Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
f8ca7e87-e5f1-4ef2-b389-02d318ccf78fAvailable on FDA.report

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

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Foaming Hand SanitizerBENZALKONIUM CHLORIDEUpLift Brands LLCf8ca7e87-e5f1-4ef2-b389-02d318ccf78f2026-03-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-118-45
ndc (product): 83986-118
ndc11 (package): 83986011845

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
83986-118-45839860118451150 mL in 1 BOTTLE, PLASTIC (83986-118-45) 1150 ml2024-02-29NoNoCurrent