Antiseptic Foaming Hand Sanitizer

Product NDC
82442-812
11-digit product format
824420812
Labeler code
82442
Product ID
82442-812_4b1f871e-4c37-6d61-e063-6294a90ae28e
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Target Corporation
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-10-11
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
Antiseptic Foaming Hand Sanitizer
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
1020365Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
93d6e4df-9428-4557-b251-c7aa9bda3412Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-812-20Antiseptic Foaming Hand Sanitizer88 mL in 1 BOTTLE, PLASTICLIQUID884
82442-812-20Antiseptic Foaming Hand Sanitizer2 in 1 CARTONLIQUID24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-812ANTISEPTIC FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [TARGET CORP.]2Current NDC, 2 package rows20241207_93d6e4df-9428-4557-b251-c7aa9bda3412.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
Antiseptic Foaming Hand SanitizerBENZALKONIUM CHLORIDETarget Corporation93d6e4df-9428-4557-b251-c7aa9bda34122026-02-18Warnings, Adverse reactionsExact identifier
ndc (product): 82442-812

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN93d6e4df-9428-4557-b251-c7aa9bda34124
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD93d6e4df-9428-4557-b251-c7aa9bda34124
1020365benzalkonium chloride 0.13 % Topical FoamSY93d6e4df-9428-4557-b251-c7aa9bda34124

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82442-812-20824420812202 BOTTLE, PLASTIC in 1 CARTON (82442-812-20) / 88 mL in 1 BOTTLE, PLASTIC2024-10-11NoNoCurrent