Cutter Brand Foaming Hand Sanitizer

Manufacturer: United Industries Corporation | Forumlated Solutions LLC
Effective date: 2020-08-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:32:42

Label at a glance#

ProductCutter Brand Foaming Hand Sanitizer

Active ingredientAlcohol

Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 59-86°F (15-30°C) Avoid freezing and excessive heat above 104°F (40°C)

Contacts and useful links#

PhoneLabel contact1-888-837-6688

Websitewww.cutterprotects.com

www.cutterprotects.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.
Contents under pressure. Do not store at temperatures above 120°F (48°C), puncture or incinerate.

Do Not Use

OTC - DO NOT USE SECTION

On children less than 2 months of age
On open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

STORAGE AND HANDLING SECTION

Store between 59-86°F (15-30°C)
Avoid freezing and excessive heat above 104°F (40°C)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Caprylic/Capric Triglyceride, Emulsifying Wax NF, Hydrofluorocarbon 152a, Isobutane, Propane, Purified Water.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-888-837-6688 or visit our website at www.cutterprotects.com

SPL UNCLASSIFIED SECTION

Distributed by Spectrum
Division of United Industries Corporation
PO Box 142642, St. Louis, MO 63114-0642

PRINCIPAL DISPLAY PANEL - 198 g Can Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cutter_™
BRAND

FOAMING
Hand
Sanitizer

LIGHTWEIGHT

EASY TO
APPLY
NO RINSE

62% ALCOHOL

Topical Solution • Antiseptic Hand Foam
Non-Sterile Solution

Net Wt 7 oz (198 g)

PRINCIPAL DISPLAY PANEL - 198 g Can Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79364-1681-3	2024-01-30	C162847	48780-1	1030e365-0910-111a-e063-dadaa90a10e2	Cutter ™ Brand Foaming Hand Sanitizer
79364-1681-6	2024-01-30	C162847	48780-1	1030e365-0910-111a-e063-dadaa90a10e2	Cutter ™ Brand Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79364-1681-3	Cutter Brand Foaming Hand Sanitizer	85 g in 1 CAN	AEROSOL, FOAM	85		1
79364-1681-6	Cutter Brand Foaming Hand Sanitizer	198 g in 1 CAN	AEROSOL, FOAM	198		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79364-1681	CUTTER BRAND FOAMING HAND SANITIZER (ALCOHOL) AEROSOL, FOAM [UNITED INDUSTRIES CORPORATION]	1	Legacy NDC, 2 package rows	20201101_2cf13e09-d0de-4c7b-8d66-8165e89be36c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Cutter Brand Foaming Hand Sanitizer
Alcohol
MEDIUM-CHAIN TRIGLYCERIDES
1,1-DIFLUOROETHANE
Isobutane
Propane
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79364-1681	79364-1681-3, 79364-1681-6

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
Name	UNII	Kind
Alcohol	3K9958V90M	ACTIB
MEDIUM-CHAIN TRIGLYCERIDES	C9H2L21V7U	IACT
1,1-DIFLUOROETHANE	0B1U8K2ME0	IACT
Isobutane	BXR49TP611	IACT
Propane	T75W9911L6	IACT
Water	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
267af434-8d1a-4ac5-9941-33b3b96d1ecf			2cf13e09-d0de-4c7b-8d66-8165e89be36c	2020-08-10	Warnings	Exact identifier spl id: 267af434-8d1a-4ac5-9941-33b3b96d1ecf spl set id: 2cf13e09-d0de-4c7b-8d66-8165e89be36c

Reported adverse events (FAERS/openFDA)#

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