Skin Soothing Hand sanitizer gel

Manufacturer: Emerge Technologies, Inc.
Effective date: 2020-09-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:29:04

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure13 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping Children under 6 years of age use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 105F May discolor fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

on open skin wounds
do not inhale or ingest
do not use on infants

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water

■Avoid contact with open skin ■ Do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops.

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
Children under 6 years of age use only under adult supervision
Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F
May discolor fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Butylene Glyool, Carbomer, Aminomethyl
Propanol, Aloe Barbadensis Leaf Extract, Xanthan Gum

Skin Soothing Hand Sanitizer Gel - 60 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 ml

Skin Soothing Hand Sanitizer Gel - 100 ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79117-075-02	2022-01-28	C162847	48780-1	d6a99b39-94e7-a426-e053-dadaa90af4c2	Skin Soothing Hand sanitizer gel
79117-075-03	2022-01-28	C162847	48780-1	d6a99b39-94e7-a426-e053-dadaa90af4c2	Skin Soothing Hand sanitizer gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79117-075-02	Hand Sanitizer	60 mL in 1 BOTTLE, DISPENSING	GEL	60		1
79117-075-03	Hand Sanitizer	100 mL in 1 BOTTLE, DISPENSING	GEL	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79117-075	HAND SANITIZER (ALCOHOL) GEL [EMERGE TECHNOLOGIES, INC.]	1	Legacy NDC, 2 package rows	20200911_af02706d-8757-3778-e053-2995a90a5e4b.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Hand Sanitizer
ALCOHOL
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ALOE VERA LEAF
BUTYLENE GLYCOL
AMINOMETHYLPROPANOL
WATER
XANTHAN GUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79117-075	79117-075-02, 79117-075-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALCOHOL	3K9958V90M	ACTIB
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
XANTHAN GUM	TTV12P4NEE	IACT

Source Document#

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
af0279f3-dd6d-27a1-e053-2a95a90a3c0f			af02706d-8757-3778-e053-2995a90a5e4b	2020-09-10	Warnings	Exact identifier spl id: af0279f3-dd6d-27a1-e053-2a95a90a3c0f spl set id: af02706d-8757-3778-e053-2995a90a5e4b

Reported adverse events (FAERS/openFDA)#

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