Alcohol-Free Hand Sanitizing Foam

Product NDC
63998-764
11-digit product format
639980764
Labeler code
63998
Product ID
63998-764_27c4d6fe-7567-073f-e063-6394a90afe9f
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
SOLUTION
Route
TOPICAL
Labeler
United Laboratories Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-01-01
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 Sanitizing Foam
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
4f5ddead-1868-45c2-9657-762c9ca3a0e2Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63998-764-01Alcohol-Free Hand Sanitizing Foam59 mL in 1 BOTTLESOLUTION592
63998-764-02Alcohol-Free Hand Sanitizing Foam750 mL in 1 BOTTLESOLUTION7502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63998-764ALCOHOL-FREE HAND SANITIZING FOAM (BENZALKONIUM CHLORIDE) SOLUTION [UNITED LABORATORIES INC.]2Current NDC, Legacy NDC, 2 package rows20241127_4f5ddead-1868-45c2-9657-762c9ca3a0e2.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 Sanitizing FoamBENZALKONIUM CHLORIDEUnited Laboratories Inc.4f5ddead-1868-45c2-9657-762c9ca3a0e22024-11-25WarningsExact identifier
ndc (product): 63998-764

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN4f5ddead-1868-45c2-9657-762c9ca3a0e22
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD4f5ddead-1868-45c2-9657-762c9ca3a0e22
1038799benzalkonium chloride 0.1 % Topical FoamSY4f5ddead-1868-45c2-9657-762c9ca3a0e22

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63998-764-016399807640159 mL in 1 BOTTLE (63998-764-01) 59 ml2019-01-010000-00-00NoNoCurrent
63998-764-0263998076402750 mL in 1 BOTTLE (63998-764-02) 750 ml2019-01-010000-00-00NoNoCurrent