Foaming Hand

Product NDC
71897-224
11-digit product format
718970224
Labeler code
71897
Product ID
71897-224_4af5534d-3be0-730d-e063-6294a90a3eaf
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOAP
Route
TOPICAL
Labeler
Veritiv Operating Company
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-08-01
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
Foaming Hand
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
3b4dbfd0-f275-3502-e063-6294a90a8486Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71897-224-86Foaming Hand1000 mL in 1 BOTTLE, PLASTICSOAP10002

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 HandBENZALKONIUM CHLORIDEVeritiv Operating Company3b4dbfd0-f275-3502-e063-6294a90a84862026-02-16Warnings, Adverse reactionsExact identifier
ndc (product): 71897-224

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN3b4dbfd0-f275-3502-e063-6294a90a84862
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD3b4dbfd0-f275-3502-e063-6294a90a84862
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY3b4dbfd0-f275-3502-e063-6294a90a84862
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY3b4dbfd0-f275-3502-e063-6294a90a84862

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71897-224-86718970224861000 mL in 1 BOTTLE, PLASTIC (71897-224-86) 1000 ml2025-08-01NoNoCurrent