Maxim Hand Sanitizer Alcohol

Manufacturer
MIDLAB INCORPORATED
Effective date
2020-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:17

Label at a glance#

ProductMaxim Hand Sanitizer Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

Principal Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal DisplayPrincipal Display

OTC Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

OTC Purpose

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Warnings

WARNINGS SECTION

WarningsWarnings

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask DoctorAsk Doctor

KOOROC

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOOROCKOOROC

Dosage

DOSAGE & ADMINISTRATION SECTION

Dosage and AdminDosage and Admin

Other Information

OTHER SAFETY INFORMATION

Other informationOther information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70542-00170542-001-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
c59cbcd4-e25e-4688-e053-2a95a90aef66ae41cb9b-6672-01b8-e053-2995a90a79ca2021-06-25WarningsExact identifier
spl set id: ae41cb9b-6672-01b8-e053-2995a90a79ca

Reported adverse events (FAERS/openFDA)#

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