CLUTCH ANTISEPTIC HAND SANITIZER

Manufacturer: MK Gas Co.
Effective date: 2020-07-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:20:20

Label at a glance#

ProductCLUTCH ANTISEPTIC HAND SANITIZER

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 83%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use
• in children less than 2 months of age
• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72 hours

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

• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

dipropylene glycol, hydrogen peroxide, water

Questions? +1-325-437-2109

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

Manufactured by: MK Gas Ltd., San Angelo Hwy, Brady, TX 76825

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MKgas1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2287157	ethanol 83 % Topical Gel	PSN	1
2287157	ethanol 0.83 ML/ML Topical Gel	SCD	1
2287157	ethyl alcohol 83 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78810-101-08	2022-01-28	C162847	48780-1	d6a99b39-c48f-a426-e053-dadaa90af4c2	CLUTCH ANTISEPTIC HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78810-101-08	CLUTCH ANTISEPTIC HAND SANITIZER	237 mL in 1 BOTTLE, PLASTIC	GEL	237		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78810-101	CLUTCH ANTISEPTIC HAND SANITIZER (ALCOHOL) GEL [MK GAS CO.]	1	Legacy NDC, 1 package rows	20200708_4e398481-349c-43a0-aa69-48be097b4635.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

CLUTCH ANTISEPTIC HAND SANITIZER
Alcohol
DIPROPYLENE GLYCOL
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78810-101	78810-101-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
DIPROPYLENE GLYCOL	E107L85C40	IACT
HYDROGEN PEROXIDE	BBX060AN9V	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
5f897cd3-5f0c-4926-a4d9-c3265ca19496			4e398481-349c-43a0-aa69-48be097b4635	2020-07-07	Warnings	Exact identifier spl id: 5f897cd3-5f0c-4926-a4d9-c3265ca19496 spl set id: 4e398481-349c-43a0-aa69-48be097b4635

Reported adverse events (FAERS/openFDA)#

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