FDA.reportPublic FDA data

Maxim Instant Foam Hand Sanitizer

Manufacturer
Midlab Incoporated | Midlab Incorporated
Effective date
2021-05-18
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 22:44:42

Label at a glance#

ProductMaxim Instant Foam Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal displayPrincipal display

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

OTC - PURPOSE SECTION

PurposePurpose

INDICATIONS & USAGE SECTION

UsesUses

WARNINGS SECTION

WarningsWarnings

OTC - ASK DOCTOR SECTION

Ask DoctorAsk Doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOOROCKOOROC

DOSAGE & ADMINISTRATION SECTION

Dosage and AdminDosage and Admin

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

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
70542-50170542-501-41, 70542-501-32, 70542-501-55

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
CITRATE ION664CCH53PIIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
ACETAMIDOETHOXYETHANOLLVX2APC4XRIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT

Source Document#

Source XML · Source PDF

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
cee27f7c-0cb9-43e3-e053-2995a90a7ee254103c39-8993-09e6-e054-00144ff8d46c2021-10-21WarningsExact identifier
spl set id: 54103c39-8993-09e6-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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