Hand Wash

Product NDC
79903-163
Requested package NDC
79903-163-32
11-digit product format
799030163
Labeler code
79903
Product ID
79903-163_4b05d712-0646-ed7f-e063-6294a90abb2e
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Walmart Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-09-14
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
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
25d227f8-2238-4f6f-aa40-b314d0179d88Available 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
79903-163-08Hand Wash3785 mL in 1 BOTTLE, PLASTICLIQUID37857
79903-163-32Hand Wash946 mL in 1 BOTTLE, PLASTICLIQUID9467
79903-163-96Hand Wash221 mL in 1 BOTTLE, PLASTICLIQUID2217

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-163HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [WALMART INC.]5Current NDC, Legacy NDC, 3 package rows20250330_25d227f8-2238-4f6f-aa40-b314d0179d88.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
Hand WashBENZALKONIUM CHLORIDEWalmart Inc.25d227f8-2238-4f6f-aa40-b314d0179d882026-02-17Warnings, Adverse reactionsExact identifier
ndc (package): 79903-163-32
ndc (product): 79903-163
ndc11 (package): 79903016332

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN25d227f8-2238-4f6f-aa40-b314d0179d887
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD25d227f8-2238-4f6f-aa40-b314d0179d887
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY25d227f8-2238-4f6f-aa40-b314d0179d887
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY25d227f8-2238-4f6f-aa40-b314d0179d887

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79903-163-3279903016332946 mL in 1 BOTTLE, PLASTIC (79903-163-32) 946 ml2022-12-150000-00-00NoNoCurrent