Advanced Hand Sanitizer

Product NDC
79903-334
Requested package NDC
79903-334-12
11-digit product format
799030334
Labeler code
79903
Product ID
79903-334_4bd4ee97-13c5-f02c-e063-6394a90a5ee6
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl 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
Advanced 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
c05bcb17-f1f6-4e3a-b90a-5d003ce5215bAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-334-03Advanced Hand Sanitizer89 mL in 1 BOTTLE, PLASTICGEL893
79903-334-12Advanced Hand Sanitizer355 mL in 1 BOTTLE, PLASTICGEL3553
79903-334-32Advanced Hand Sanitizer946 mL in 1 BOTTLE, PLASTICGEL9463
79903-334-60Advanced Hand Sanitizer1770 mL in 1 BOTTLE, PLASTICGEL17703

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79903-334ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [WALMART INC.]2Current NDC, 4 package rows20250311_c05bcb17-f1f6-4e3a-b90a-5d003ce5215b.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
Advanced Hand SanitizerETHYL ALCOHOLWalmart Inc.c05bcb17-f1f6-4e3a-b90a-5d003ce5215b2026-02-27Warnings, Adverse reactionsExact identifier
ndc (package): 79903-334-12
ndc (product): 79903-334
ndc11 (package): 79903033412

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSNc05bcb17-f1f6-4e3a-b90a-5d003ce5215b3
581662ethanol 0.7 ML/ML Topical GelSCDc05bcb17-f1f6-4e3a-b90a-5d003ce5215b3
581662ethanol 70 % Topical GelSYc05bcb17-f1f6-4e3a-b90a-5d003ce5215b3
581662ethyl alcohol 70 % Topical GelSYc05bcb17-f1f6-4e3a-b90a-5d003ce5215b3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
79903-334-1279903033412355 mL in 1 BOTTLE, PLASTIC (79903-334-12) 355 ml2025-03-10NoNoCurrent