FDA.reportPublic FDA data

Hand Wash

Product NDC
69790-466
11-digit product format
697900466
Labeler code
69790
Product ID
69790-466_4b099bfa-cd9d-d843-e063-6294a90accae
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
SOAP
Route
TOPICAL
Labeler
ULINE
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-02-17
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
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
5a4d6fb7-486a-448c-b379-726adf60e411Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69790-466-962022-08-26C16284748780-1e4f33bdf-9f3e-d8a0-e053-dadaa90a6e4eUline 466.001/466AB Antibacterial Foaming Hand Wash
69790-466-962022-07-29C16284748780-1e4f33bdf-9f3e-d8a0-e053-dadaa90a6e4eUline 466.001/466AB Antibacterial Foaming Hand Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69790-466-96Hand Wash221 mL in 1 BOTTLE, PLASTICSOAP22112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69790-466HAND WASH (BENZALKONIUM CHLORIDE) SOAP [ULINE]10Current NDC, Legacy NDC, 1 package rows20240929_5a4d6fb7-486a-448c-b379-726adf60e411.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 CHLORIDEULINE5a4d6fb7-486a-448c-b379-726adf60e4112026-02-17Warnings, Adverse reactionsExact identifier
ndc (product): 69790-466

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN5a4d6fb7-486a-448c-b379-726adf60e41112
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD5a4d6fb7-486a-448c-b379-726adf60e41112
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY5a4d6fb7-486a-448c-b379-726adf60e41112
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY5a4d6fb7-486a-448c-b379-726adf60e41112

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69790-466-9669790046696221 mL in 1 BOTTLE, PLASTIC (69790-466-96) 221 ml2016-02-170000-00-00NoNoCurrent