SSDC ANTIBACTERIAL FOAM HANDSOAP

Product NDC
47593-663
11-digit product format
475930663
Labeler code
47593
Product ID
47593-663_f69d870e-1eba-4623-ac25-e8fbb0a66e8f
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Ecolab Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-03-03
Substance
BENZALKONIUM CHLORIDE
Active strength
5 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
SSDC ANTIBACTERIAL FOAM HANDSOAP
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE5 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
1731737Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a2a4e9d1-d63a-476b-a048-d360104e3688Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-663-70SSDC ANTIBACTERIAL FOAM HANDSOAP1200 mL in 1 BOTTLE, PLASTICSOLUTION12001

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
SSDC ANTIBACTERIAL FOAM HANDSOAPBENZALKONIUM CHLORIDEEcolab Inc.a2a4e9d1-d63a-476b-a048-d360104e36882026-03-03WarningsExact identifier
ndc (product): 47593-663

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSNa2a4e9d1-d63a-476b-a048-d360104e36881
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCDa2a4e9d1-d63a-476b-a048-d360104e36881
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSYa2a4e9d1-d63a-476b-a048-d360104e36881

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
47593-663-70475930663701200 mL in 1 BOTTLE, PLASTIC (47593-663-70) 1200 ml2026-03-03NoNoCurrent