Antibacterial Hand Wash

Product NDC
83986-015
11-digit product format
839860015
Labeler code
83986
Product ID
83986-015_4cc5aeaf-48f4-d9fb-e063-6394a90adc56
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
SOAP
Route
TOPICAL
Labeler
UpLift Brands LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-10-14
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

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
Antibacterial Hand Wash
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
1046593Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2e9a5253-f68d-4db5-a479-2663fc7789afAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-015-32Antibacterial Hand Wash355 mL in 1 BOTTLE, PUMPSOAP3553

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83986-015ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE) SOAP [UPLIFT BRANDS LLC]1Current NDC, 1 package rows20240310_2e9a5253-f68d-4db5-a479-2663fc7789af.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
Antibacterial Hand WashBENZALKONIUM CHLORIDEUpLift Brands LLC2e9a5253-f68d-4db5-a479-2663fc7789af2026-03-11Warnings, Adverse reactionsExact identifier
ndc (product): 83986-015

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2e9a5253-f68d-4db5-a479-2663fc7789af3
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2e9a5253-f68d-4db5-a479-2663fc7789af3
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2e9a5253-f68d-4db5-a479-2663fc7789af3
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2e9a5253-f68d-4db5-a479-2663fc7789af3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83986-015-3283986001532355 mL in 1 BOTTLE, PUMP (83986-015-32) 355 ml2022-10-14NoNoCurrent