FDA.reportPublic FDA data

I2Pure Hand Sanitizer

Manufacturer
I2Pure Corp. | I2Pure Corp
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:29:06

Label at a glance#

ProductI2Pure Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

PurposePurpose

DOSAGE & ADMINISTRATION SECTION

DosageDosage

WARNINGS SECTION

WarningWarning

INACTIVE INGREDIENT SECTION

Inactive INgredientsInactive INgredients

INDICATIONS & USAGE SECTION

IndicationIndication

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reachKeep out of reach

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PrinicpalPrinicpal

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN3
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD3
808520isopropyl alcohol 70 % Topical SolutionSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83465-321-01I2Pure Hand Sanitizer30 mL in 1 BOTTLE, PLASTICLIQUID303
83465-321-08I2Pure Hand Sanitizer240 mL in 1 BOTTLE, PLASTICLIQUID2403
83465-321-16I2Pure Hand Sanitizer480 mL in 1 BOTTLE, PLASTICLIQUID4803

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83465-32183465-321-08, 83465-321-01, 83465-321-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYDROXYPROPYL METHYLCELLULOSE3NXW29V3WOIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
IODINE9679TC07X4IACT
POLYETHYLENE GLYCOL 8000Q662QK8M3BIACT
SODIUM IODIDEF5WR8N145CIACT

Source Document#

Source XML

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
47195b96-dc17-3001-e063-6294a90a23fe2a949a9b-4d4a-037a-e063-6394a90a75ad2025-12-29WarningsExact identifier
spl id: 47195b96-dc17-3001-e063-6294a90a23fe
spl set id: 2a949a9b-4d4a-037a-e063-6394a90a75ad

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.