70% alcohol hand sanitzer

Manufacturer: D Zone Imports, Llc
Effective date: 2020-06-25
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:19:05

Label at a glance#

Product70% alcohol hand sanitzer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using.

Storage and handling

Store at room temperature May discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% 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

When using this product

OTC - WHEN USING SECTION

Avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature
May discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerol, Carbopol, Triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 75021-003-01

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75021-003-01	2022-01-28	C162847	48780-1	d6a99b39-aa4b-a426-e053-dadaa90af4c2	70% alcohol hand sanitzer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75021-003-01	70% alcohol hand sanitzer	60 mL in 1 BOTTLE	GEL	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75021-003	70% ALCOHOL HAND SANITZER (ALCOHOL) GEL [D ZONE IMPORTS, LLC]	2	Legacy NDC, 1 package rows	20200626_a863d7c6-35e9-d8eb-e053-2a95a90a33d3.zip

Products#

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

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

70% alcohol hand sanitzer
ALCOHOL
GLYCERIN
TROLAMINE
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75021-003	75021-003-01
56084-020

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
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
a8e31de9-7ac0-9669-e053-2995a90a5b83			a863d7c6-35e9-d8eb-e053-2a95a90a33d3	2020-06-25	Warnings	Exact identifier spl id: a8e31de9-7ac0-9669-e053-2995a90a5b83 spl set id: a863d7c6-35e9-d8eb-e053-2a95a90a33d3

Reported adverse events (FAERS/openFDA)#

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