Freeman Packaging Hand Sanitizer

Product NDC
71734-201
Requested package NDC
71734-201-01
11-digit product format
717340201
Labeler code
71734
Product ID
71734-201_972b3dde-977d-4b7f-8a01-03797f92087a
Type
HUMAN OTC DRUG
Nonproprietary name
ALCOHOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2017-10-09
Substance
ALCOHOL
Active strength
62 mL/100mL
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
Freeman Packaging Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL62 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
247835Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
9827418a-3ab6-447b-8f8a-9eacb56d3a89Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71734-201-01Freeman Packaging Hand Sanitizer7.5 mL in 1 BOTTLELIQUID7.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71734-201FREEMAN PACKAGING HAND SANITIZER (ALCOHOL) LIQUID [JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.]1Current NDC, Legacy NDC, 1 package rows20171010_9827418a-3ab6-447b-8f8a-9eacb56d3a89.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
Freeman Packaging Hand SanitizerALCOHOLJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.9827418a-3ab6-447b-8f8a-9eacb56d3a892017-10-09WarningsExact identifier
ndc (package): 71734-201-01
ndc (product): 71734-201
ndc11 (package): 71734020101

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
247835ethanol 62 % Topical SolutionPSN9827418a-3ab6-447b-8f8a-9eacb56d3a891
247835ethanol 0.62 ML/ML Topical SolutionSCD9827418a-3ab6-447b-8f8a-9eacb56d3a891
247835ethanol 62 % Topical SolutionSY9827418a-3ab6-447b-8f8a-9eacb56d3a891
247835ethyl alcohol 62 % Topical SolutionSY9827418a-3ab6-447b-8f8a-9eacb56d3a891

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71734-201-01717340201017.5 mL in 1 BOTTLE (71734-201-01) 7.5 ml2017-10-090000-00-00NoNoCurrent