FDA.reportPublic FDA data

Alcohol Free Hand Sanitizer

Product NDC
60933-200
11-digit product format
609330200
Labeler code
60933
Product ID
60933-200_08c07ef8-6cc8-bd48-e063-6294a90a51b9
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
FULLER INDUSTRIES, INC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-09-01
Substance
BENZALKONIUM CHLORIDE
Active strength
1 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Alcohol Free Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1 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
1038799Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0ebf85c5-21ee-4d14-b88f-d8c078791aefAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60933-200-00Alcohol Free Hand Sanitizer1000 mL in 1 BAGAEROSOL, FOAM10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60933-200ALCOHOL FREE HAND SANITIZER (BENZALKONIUM CHLORIDE) AEROSOL, FOAM [FULLER INDUSTRIES, INC]4Current NDC, Legacy NDC, 1 package rows20231030_0ebf85c5-21ee-4d14-b88f-d8c078791aef.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
Alcohol Free Hand SanitizerBENZALKONIUM CHLORIDEFULLER INDUSTRIES, INC0ebf85c5-21ee-4d14-b88f-d8c078791aef2023-10-28WarningsExact identifier
ndc (product): 60933-200

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN0ebf85c5-21ee-4d14-b88f-d8c078791aef4
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD0ebf85c5-21ee-4d14-b88f-d8c078791aef4
1038799benzalkonium chloride 0.1 % Topical FoamSY0ebf85c5-21ee-4d14-b88f-d8c078791aef4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60933-200-00609330200001000 mL in 1 BAG (60933-200-00) 1000 ml2017-09-010000-00-00NoNoCurrent