Hand Sanitizer

Manufacturer: K7 Design Group Inc.
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:57:48

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure6 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hanw-ashing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

For external use onlyFlammable, keep away from fire and flames.

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Contorl Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Glycerin, Carbomer, Triethanolamine, Denatonium Benzoate.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	2
581660	ethanol 0.62 ML/ML Topical Gel	SCD	2
581660	ethanol 62 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74177-021-00	Hand Sanitizer	236 mL in 1 BOTTLE	GEL	236		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74177-021	HAND SANITIZER (ALCOHOL) GEL [K7 DESIGN GROUP INC.]	2	Current NDC, Legacy NDC, 1 package rows	20231026_a4e65bc9-3a84-142c-e053-2995a90ade6a.zip

Products#

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

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

Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
DENATONIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74177-021	74177-021-00

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
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Hand Sanitizer	ALCOHOL	K7 Design Group Inc.	a4e65bc9-3a84-142c-e053-2995a90ade6a	2023-10-26	Warnings	Exact identifier ndc (package): 74177-021-00 ndc (product): 74177-021 ndc11 (package): 74177002100 spl id: 08979f64-b260-9491-e063-6294a90a5fa7 spl set id: a4e65bc9-3a84-142c-e053-2995a90ade6a

Reported adverse events (FAERS/openFDA)#

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