FDA.reportPublic FDA data

HAND-I-SAN

Product NDC
85820-900
Requested package NDC
85820-900-03
11-digit product format
858200900
Labeler code
85820
Product ID
85820-900_37627a51-cf32-013c-e063-6294a90ae13a
Type
HUMAN OTC DRUG
Nonproprietary name
75% Isopropyl Alcohol Hand Sanitizer
Dosage form
LIQUID
Route
TOPICAL
Labeler
ZECO, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-13
Substance
ISOPROPYL ALCOHOL
Active strength
.75 L/L
NDC exclude flag
No
Listing certified through
2026-12-31
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-I-SAN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ISOPROPYL ALCOHOL.75 L/L

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
ND2M416302Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1039900Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
37627a51-cf31-013c-e063-6294a90ae13aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85820-900-01HAND-I-SAN3.78 L in 1 JUGLIQUID3.781
85820-900-02HAND-I-SAN18.29 L in 1 PAILLIQUID18.291
85820-900-03HAND-I-SAN208.17 L in 1 DRUMLIQUID208.171
85820-900-04HAND-I-SAN1040.87 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID1040.871
85820-900-11HAND-I-SAN4 in 1 BOXLIQUID41

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-I-SAN75% ISOPROPYL ALCOHOL HAND SANITIZERZECO, LLC37627a51-cf31-013c-e063-6294a90ae13a2025-06-13WarningsExact identifier
ndc (package): 85820-900-03
ndc (product): 85820-900
ndc11 (package): 85820090003

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1039900isopropyl alcohol 75 % Topical SolutionPSN37627a51-cf31-013c-e063-6294a90ae13a1
1039900isopropyl alcohol 0.75 ML/ML Topical SolutionSCD37627a51-cf31-013c-e063-6294a90ae13a1
1039900isopropyl alcohol 75 % Topical SolutionSY37627a51-cf31-013c-e063-6294a90ae13a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85820-900-0385820090003208.17 L in 1 DRUM (85820-900-03) 208.17 l2025-06-13NoNoCurrent