Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Storage and handling

Other information Store between 15-30°C（59-86°F） Avoid freezing and excessive heat above 40°C (104°F) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient[s]
Ethyl Alcohol 75% v/v

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Use[s]

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS SECTION

Warnings

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

OTC - DO NOT USE SECTION

Do not use

• in children less than 2 months of age

• on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.

STORAGE AND HANDLING SECTION

Other information

Store between 15-30°C（59-86°F）
Avoid freezing and excessive heat above 40°C (104°F)
May discolor certain fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water (Aqua), Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Denatonium Benzoate, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Maltodextrin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1305100	Ethanol (Topical)	ethanol 0.75 ML/ML Topical Gel	SCD Active

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
78702-335-01	2025-01-30	C162847	48780-1	2cef2736-b27a-d83d-e063-dadaa90ab31f	a96e0b99-c6d2-148b-e053-2995a90a490f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78702-335-01	Hand Sanitizer	991 mL in 1 BOTTLE, PUMP	GEL	991		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78702-335	HAND SANITIZER (ETHYL ALCOHOL) GEL [TASTEK LLC]	1	Legacy NDC, 1 package rows	20200702_a96e0b99-c6d2-148b-e053-2995a90a490f.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Hand Sanitizer
ETHYL ALCOHOL
MALTODEXTRIN
PROPYLENE GLYCOL
WATER
ALOE VERA LEAF
GLYCERIN
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
.ALPHA.-TOCOPHEROL ACETATE
AMINOMETHYLPROPANOL
DENATONIUM BENZOATE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78702-335	78702-335-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MALTODEXTRIN	7CVR7L4A2D	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	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
a96e0990-52b9-2b8f-e053-2995a90a8eae			a96e0b99-c6d2-148b-e053-2995a90a490f	2020-07-01	Warnings	Exact identifier spl id: a96e0990-52b9-2b8f-e053-2995a90a8eae spl set id: a96e0b99-c6d2-148b-e053-2995a90a490f

Reported adverse events (FAERS/openFDA)#

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

Hand Sanitizer