Hand Sanitizer

Product NDC
79903-335
11-digit product format
799030335
Labeler code
79903
Product ID
79903-335_4bd4cd8e-8b92-cab0-e063-6394a90a052b
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
Walmart Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-03-10
Substance
ALCOHOL
Active strength
70 mL/100mL
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
Hand Sanitizer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL70 mL/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
581662Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2112ba04-1584-46dd-9a7b-2dfd27e501b7Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-335-12Hand Sanitizer355 mL in 1 BOTTLE, PUMPGEL3553
79903-335-32Hand Sanitizer946 mL in 1 BOTTLE, PUMPGEL9463
79903-335-60Hand Sanitizer1770 mL in 1 BOTTLE, PUMPGEL17703

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-335HAND SANITIZER (ALCOHOL) GEL [WALMART INC.]2Current NDC, 3 package rows20250311_2112ba04-1584-46dd-9a7b-2dfd27e501b7.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
Hand SanitizerALCOHOLWalmart Inc.2112ba04-1584-46dd-9a7b-2dfd27e501b72026-02-27Warnings, Adverse reactionsExact identifier
ndc (product): 79903-335

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN2112ba04-1584-46dd-9a7b-2dfd27e501b73
581662ethanol 0.7 ML/ML Topical GelSCD2112ba04-1584-46dd-9a7b-2dfd27e501b73
581662ethanol 70 % Topical GelSY2112ba04-1584-46dd-9a7b-2dfd27e501b73
581662ethyl alcohol 70 % Topical GelSY2112ba04-1584-46dd-9a7b-2dfd27e501b73

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-335-1279903033512355 mL in 1 BOTTLE, PUMP (79903-335-12) 355 ml2025-03-10NoNoCurrent
79903-335-3279903033532946 mL in 1 BOTTLE, PUMP (79903-335-32) 946 ml2025-03-10NoNoCurrent
79903-335-60799030335601770 mL in 1 BOTTLE, PUMP (79903-335-60) 1770 ml2025-03-10NoNoCurrent