Instant Hand Sanitizer

Manufacturer: Graphic Controls | Safetec of America, Inc. | Safetec of America, Inc
Effective date: 2009-11-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:22:50

Label at a glance#

ProductInstant Hand Sanitizer

Active ingredientAlcohol

Label structure8 sections

Indications and uses

for handwashing to decrease bacteria on skin recommended for repeated use

Dosage and administration

wet hands thorough with product allow to dry without wiping children under 6 should be supervised while using this product

Contacts and useful links#

PhoneLabel contact1-800-669-1535

PhoneLabel contact800-665-1535

Websitewww.graphiccontrols.com

www.graphiccontrols.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

Pupose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on skin
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use in the eyes. If this happens, rinse thoroughly with water

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thorough with product
allow to dry without wiping
children under 6 should be supervised while using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Manufactured for Graphic Controls LLC
Buffalo, NY 14204
1-800-669-1535

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL – BOTTLE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FREE Sample-Not for Resale

GRAPHIC CONTROLS LLC – Instant Hand Sanitizer

For more information or To Order call

800-665-1535

www.graphiccontrols.com

Kills 99.99% of Germs

Enriched with Aloe Vera

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL – BOTTLE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616762	ethanol 66.5 % Topical Gel	PSN	2
616762	ethanol 0.665 ML/ML Topical Gel	SCD	2
616762	ethanol 66.5 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49959-1111-0	2020-01-31	C162847	48780-1	9d75b9cf-d904-f424-e053-dadaa90a57ce	Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49959-1111-0	Instant Hand Sanitizer	59 mL in 1 BOTTLE	GEL	59		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49959-1111	INSTANT HAND SANITIZER (ALCOHOL) GEL [GRAPHIC CONTROLS]	2	Legacy NDC, 1 package rows	20091130_c298118e-ff72-4dcc-8804-9c1f4b6a46b5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Alcohol	ACTIVE INGREDIENT	3K9958V90M	2
Alcohol	ACTIVE MOIETY	3K9958V90M	2
Aloe	INACTIVE INGREDIENT	V5VD430YW9	2
D&C Green No. 5	INACTIVE INGREDIENT	8J6RDU8L9X	2
D&C Yellow No. 10	INACTIVE INGREDIENT	35SW5USQ3G	2
Water	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Instant Hand Sanitizer
Alcohol
Aloe
D&C Green No. 5
D&C Yellow No. 10
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49959-1111	49959-1111-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Alcohol	3K9958V90M	ACTIB
Aloe	V5VD430YW9	IACT
D&C Green No. 5	8J6RDU8L9X	IACT
D&C Yellow No. 10	35SW5USQ3G	IACT
Water	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 37 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, EXTENDED RELEASE / ORAL		14 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	GEL / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, CHEWABLE / ORAL		4 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SYRUP / ORAL		4 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	SOAP / TOPICAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	TABLET / ORAL	0.03 mg		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SHAMPOO / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	LOTION / TOPICAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE / ORAL	20 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET / ORAL	80 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	GUM, CHEWING / BUCCAL		24 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, DELAYED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CONCENTRATE / ORAL	0.03 mg/1ml		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUSPENSION, EXTENDED RELEASE / ORAL		1 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, DELAYED RELEASE / ORAL	1.9 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOLUTION / RECTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOLUTION / ORAL		8 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, COATED PELLETS / ORAL	0.01 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, COATED / ORAL	2.5 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	ELIXIR / ORAL	0.3 mg/15ml		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET / SUBLINGUAL	0.23 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, EXTENDED RELEASE / ORAL		3 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	TABLET, FILM COATED / ORAL	120 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	GUM, CHEWING / ORAL		2 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SOAP / TOPICAL	1.4 %w/w		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	CAPSULE, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	GEL / DENTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER / ORAL		48 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	PASTE / DENTAL	NA		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	SHAMPOO / TOPICAL	0.09 %w/w		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUPPOSITORY / RECTAL	0.11 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	SUSPENSION / ORAL	20 mg/5ml		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	SOLUTION / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	CAPSULE, LIQUID FILLED / ORAL	1.51 mg		Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Yellow No. 10	D&C YELLOW NO. 10	35SW5USQ3G	POWDER, FOR SUSPENSION / ORAL		76 mg	Exact identifier — unii candidate 31 equally ranked IID candidates
D&C Green No. 5	D&C GREEN NO. 5	8J6RDU8L9X	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 6 equally ranked IID candidates

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
8b28802d-c750-4607-a01c-4ebaa25e115f			c298118e-ff72-4dcc-8804-9c1f4b6a46b5	2009-11-09	Warnings	Exact identifier spl id: 8b28802d-c750-4607-a01c-4ebaa25e115f spl set id: c298118e-ff72-4dcc-8804-9c1f4b6a46b5

Reported adverse events (FAERS/openFDA)#

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