Aramark Hand Sanitizer

Manufacturer: Western First Aid Safety DBA Aramark | Safetec of America, Inc.
Effective date: 2021-05-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:40:28

Label at a glance#

ProductAramark Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

■ for hand washing to decrease bacteria on skin without soap and water ■ recommended for repeated use

Dosage and administration

■ wet hands and wrists thoroughly with product and allow to dry without wiping ■ children under 6 years of age should be supervised while using this product

Contacts and useful links#

PhoneLabel contact(913) 269-9611

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

■ for hand washing to decrease bacteria on skin without soap and water

■ recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable., keep away from fire or flame.

Do not use in eyes.

OTC - DO NOT USE SECTION

If this happens, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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 and wrists thoroughly with product and allow to dry without wiping

■ children under 6 years of age 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

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

aramark

25 ct. _{Each Packet Net. Wt. 0.9g}

HAND SANITIZER

Kills 99.9% of Germs

Enriched with Aloe Vera

NDC 81238-1112-2

aramarkuniform.com

MANUFACTURED FOR:

Aramark

Lenexa, KS 66219

(913) 269-9611

Please retain carton for drug information.

1112-2 25ct Box

1112-2 Packet

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616762	ethanol 66.5 % Topical Gel	PSN	1
616762	ethanol 0.665 ML/ML Topical Gel	SCD	1
616762	ethanol 66.5 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81238-1112-2	2023-01-30	C162847	48780-1	f386c64a-30ad-0266-e053-dadaa90a7c1a	aramark Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81238-1112-2	Aramark Hand Sanitizer	25 in 1 BOX	GEL	25		1
81238-1112-2	Aramark Hand Sanitizer	0.9 mL in 1 PACKET	GEL	0.9		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81238-1112	ARAMARK HAND SANITIZER (ALCOHOL) GEL [WESTERN FIRST AID SAFETY DBA ARAMARK]	1	Legacy NDC, 2 package rows	20210522_7d4cbaf6-d6f8-4c31-b3a3-ecd4d86d8cad.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Aramark Hand Sanitizer
ALCOHOL
ALOE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
D&C GREEN NO. 5
D&C YELLOW NO. 10
WATER
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81238-1112	81238-1112-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
ALOE	V5VD430YW9	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
D&C GREEN NO. 5	8J6RDU8L9X	IACT
D&C YELLOW NO. 10	35SW5USQ3G	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	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
ece7cbc0-e4a7-4a57-bcf6-893ea94bcbaa			7d4cbaf6-d6f8-4c31-b3a3-ecd4d86d8cad	2021-05-20	Warnings	Exact identifier spl id: ece7cbc0-e4a7-4a57-bcf6-893ea94bcbaa spl set id: 7d4cbaf6-d6f8-4c31-b3a3-ecd4d86d8cad

Reported adverse events (FAERS/openFDA)#

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