Label at a glance#

ProductHAND SANITIZER

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6 years of age only under adult supervision.

Storage and handling

Store between 15-30℃(59-86℉). Avoid freezing and excessive heat above 40℃(104℉).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

70% Alcohol

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.
Flammable.
May discolor some fabrics.
Harmful to wood finishes and plastics.

OTC - WHEN USING SECTION

Keep out of eyes, in case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical help 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 years of age only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30℃(59-86℉).
Avoid freezing and excessive heat above 40℃(104℉).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Tocopheryl Acetate, Vanilla Bean Aromatica.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL in 1 BOTTLE, NDC: 79931-001-01 30ml label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1041849	ethanol 0.7 ML/ML Topical Spray	ethanol 0.7 ML/ML Topical Spray	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	2
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	2
1041849	ethanol 70 % Topical Spray	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79931-001-01	2023-07-28	C162847	48780-1	0191ceaa-66b6-198a-e063-dbdaa90aec3e	Steel Supplements, Inc. 30mL HAND SANITIZER 79931-001-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79931-001-01	HAND SANITIZER	30 mL in 1 BOTTLE	SPRAY	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79931-001	HAND SANITIZER SPRAY [STEEL SUPPLEMENTS, INC.]	2	Legacy NDC, 1 package rows	20220106_abbfd6a1-a6e7-7def-e053-2995a90adb6a.zip

Products#

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

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

HAND SANITIZER
VANILLA BEAN
GLYCERIN
TOCOPHEROL
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79931-001	79931-001-01

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
VANILLA BEAN	Q74T35078H	IACT
GLYCERIN	PDC6A3C0OX	IACT
TOCOPHEROL	R0ZB2556P8	IACT
WATER	059QF0KO0R	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
d4d6fbb7-52c6-64c5-e053-2995a90ae209			abbfd6a1-a6e7-7def-e053-2995a90adb6a	2022-01-05	Warnings	Exact identifier spl id: d4d6fbb7-52c6-64c5-e053-2995a90ae209 spl set id: abbfd6a1-a6e7-7def-e053-2995a90adb6a

Reported adverse events (FAERS/openFDA)#

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

HAND SANITIZER