FDA.reportPublic FDA data

FoamyiQ Non-Alcohol Hand Sanitizer

Product NDC
64009-221
11-digit product format
640090221
Labeler code
64009
Product ID
64009-221_56cea4e7-c425-e6bd-e063-6394a90a498d
Type
HUMAN OTC DRUG
Nonproprietary name
FoamyiQ Non-Alcohol Hand Sanitizer
Dosage form
SOAP
Route
TOPICAL
Labeler
Spartan Chemical Company
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-12-31
Substance
BENZALKONIUM CHLORIDE
Active strength
1 g/1000g
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
FoamyiQ Non-Alcohol Hand Sanitizer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1 g/1000g

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
1038791Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
ee8a2af2-0572-19b1-e053-2995a90a23aeAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64009-221-06FoamyiQ Non-Alcohol Hand Sanitizer1250 g in 1 CONTAINERSOAP12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64009-221FOAMYIQ NON-ALCOHOL HAND SANITIZER SOAP [SPARTAN CHEMICAL COMPANY]2Current NDC, Legacy NDC, 1 package rows20231220_ee8a2af2-0572-19b1-e053-2995a90a23ae.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 115 of 115 · 2,286 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Povidone-Iodine PadPOVIDONE-IODINEShandong Haiyan Medical Manufacture Co., Ltd.c9187a07-92d5-15ac-e053-2995a90af4cb2022-03-19WarningsExact identifier
application number: M003
Alcohol Prep PadISOPROPYL ALCOHOLShandong Haiyan Medical Manufacture Co., Ltd.1a117840-22d0-4a88-b1a6-e43162a444ab2022-03-19WarningsExact identifier
application number: M003
FIRSTAR BZK Antiseptic ToweletteBENZALKONIUM CHLORIDEJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.28591a97-9291-48c8-a8e3-c419180331b32021-07-06WarningsExact identifier
application number: M003
Bactine MaxBENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDEWellSpring Pharmaceutical Corporation28e8a311-20a4-45a1-8d5d-ca42b101c2752021-02-24WarningsExact identifier
application number: M003
Hand Sanitizer Lemon 2ozALCOHOLNingbo Rejoice Internationalb0a4159a-cb07-4ce6-e053-2995a90a76e72020-10-02WarningsExact identifier
application number: M003
Sanix Alcohol Hand RubALCOHOLTopiderm, Inca4fbb714-4f20-400a-ab98-f1c8807ce6fc2020-03-24WarningsExact identifier
application number: M003

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1038791benzalkonium chloride 0.1 % Topical SolutionPSNee8a2af2-0572-19b1-e053-2995a90a23ae2
1038791benzalkonium chloride 1 MG/ML Topical SolutionSCDee8a2af2-0572-19b1-e053-2995a90a23ae2
1038791benzalkonium chloride 0.1 % Topical SolutionSYee8a2af2-0572-19b1-e053-2995a90a23ae2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64009-221-06640090221061250 g in 1 CONTAINER (64009-221-06) 1250 g2022-12-310000-00-00NoNoCurrent