Ethyl Alcohol

Manufacturer: PROGRESSIVE PRODUCTS, LLC
Effective date: 2022-10-14
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:51:01

Label at a glance#

ProductEthyl Alcohol

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Apply topically to the skin to help prevent cross contamination. Not recommended for repeated use. Dries in seconds

Dosage and administration

Pull back reseal label. Remover wipe. Reseal label Keep label closed to retain moisture.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin.
Apply topically to the skin to help prevent cross contamination.
Not recommended for repeated use.
Dries in seconds

Warnings

WARNINGS SECTION

For external use only.

Flammable

SAFE HANDLING WARNING SECTION

keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in or near the eyes
on open skin wounds or burns.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop
condition persists for more than 72 hours.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pull back reseal label.
Remover wipe.
Reseal label
Keep label closed to retain moisture.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature.
Dispose of used wipe in trash, do not flush into toilet.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Fragrance, Benzalkonium Chloride, Tocopheryl Acetate, Citric Acid, Aloe Barbadensis Extract.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wipesplus

SANITIZING WIPES

80CT

PRE-MOISTENED TOWELETTES

WIPES PLUS

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1489307	ethanol 70 % Medicated Pad	PSN	3
1489307	ethanol 0.7 ML/ML Medicated Pad	SCD	3
1489307	ethanol 70 % Medicated Pad	SY	3
1489307	ethanol 70 % Medicated Wipes	SY	3
1489307	ethyl alcohol 70 % Cloth	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
67151-707-01	2024-01-30	C162847	48780-1	1030e365-226b-111a-e063-dadaa90a10e2	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67151-707-01	Ethyl Alcohol	80 in 1 POUCH	SWAB	80		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67151-707	ETHYL ALCOHOL (WIPES PLUS) SWAB [PROGRESSIVE PRODUCTS, LLC]	3	Legacy NDC, 1 package rows	20221015_d82bfa06-2426-f369-e053-2995a90af622.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Ethyl Alcohol
Wipes Plus
PROPYLENE GLYCOL
BENZALKONIUM CHLORIDE
CITRIC ACID MONOHYDRATE
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67151-707	67151-707-01

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
PROPYLENE GLYCOL	6DC9Q167V3	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALOE VERA LEAF	ZY81Z83H0X	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
eaff350e-0959-261b-e053-2995a90a6be0			d82bfa06-2426-f369-e053-2995a90af622	2022-10-14	Warnings	Exact identifier spl id: eaff350e-0959-261b-e053-2995a90a6be0 spl set id: d82bfa06-2426-f369-e053-2995a90af622

Reported adverse events (FAERS/openFDA)#

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