Hand Sanitizer

Manufacturer: S.F. & B. COLOR MATES CORP.
Effective date: 2020-04-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:16

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

■ To decrease bacteria on the skin that could cause disease. ■ Recommended for repeated use

Dosage and administration

■ Wet hands thoroughly with product and allow to dry without wiping ■ For children under 6, use only under adult supervision ■ Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ To decrease bacteria on the skin that could cause disease. ■ Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only-hands. Flammable. Keep away from heat or flame.

When using this product

OTC - WHEN USING SECTION

■ Keep out of eyes. In case of contact with eyes, flush throughly with water. ■ Do not inhale or ingest. ■ Avoid contact with broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

if skin irritation develops.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet hands thoroughly with product and allow to dry without wiping ■ For children under 6, use only under adult supervision ■ Not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

■ Do not store above105ºF ■ May discolor some fabrics ■ Harmful to wood finishes and plastics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aminomethylpropanol, Aloe Barbadensis Extract

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	1
902574	ethanol 0.65 ML/ML Topical Gel	SCD	1
902574	ethyl alcohol 65 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76781-001-02	2022-01-28	C162847	48780-1	d6a99b39-d82d-a426-e053-dadaa90af4c2	Colormates Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76781-001-02	Hand Sanitizer	59 mL in 1 BOTTLE, PLASTIC	GEL	59		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76781-001	HAND SANITIZER (ALCOHOL) GEL [S.F. & B. COLOR MATES CORP.]	1	Legacy NDC, 1 package rows	20200428_a40b17f7-49f1-467c-e053-2a95a90a6aee.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
GLYCERIN
AMINOMETHYLPROPANOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76781-001	76781-001-02

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
GLYCERIN	PDC6A3C0OX	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
a40b15bd-231d-4485-e053-2995a90ad846			a40b17f7-49f1-467c-e053-2a95a90a6aee	2020-04-24	Warnings	Exact identifier spl id: a40b15bd-231d-4485-e053-2995a90ad846 spl set id: a40b17f7-49f1-467c-e053-2a95a90a6aee

Reported adverse events (FAERS/openFDA)#

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