Hand Wash

Product NDC
41250-661
Requested package NDC
41250-661-96
11-digit product format
412500661
Labeler code
41250
Product ID
41250-661_4b33dcaa-f3c2-467e-e063-6294a90a4e16
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Meijer, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-12-20
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
8fbbc798-ac00-4755-a2c2-5cd5b5c01ae4Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-661-45Hand Wash946 mL in 1 BOTTLE, PLASTICLIQUID94614
41250-661-96Hand Wash221 mL in 1 BOTTLE, PUMPLIQUID22114

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-661HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [MEIJER DISTRIBUTION, INC]12Current NDC, Legacy NDC, 2 package rows20250311_8fbbc798-ac00-4755-a2c2-5cd5b5c01ae4.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 CHLORIDEMeijer, Inc.8fbbc798-ac00-4755-a2c2-5cd5b5c01ae42026-02-19Warnings, Adverse reactionsExact identifier
ndc (package): 41250-661-96
ndc (product): 41250-661
ndc11 (package): 41250066196

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN8fbbc798-ac00-4755-a2c2-5cd5b5c01ae414
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD8fbbc798-ac00-4755-a2c2-5cd5b5c01ae414
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY8fbbc798-ac00-4755-a2c2-5cd5b5c01ae414
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY8fbbc798-ac00-4755-a2c2-5cd5b5c01ae414

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-661-9641250066196221 mL in 1 BOTTLE, PUMP (41250-661-96) 221 ml2019-12-200000-00-00NoNoCurrent