Alcohol

Manufacturer: United Natural Foods, Inc. dba UNFI | Nice-Pak Products, LLC
Effective date: 2026-02-17
Label type: HUMAN OTC DRUG LABEL
Version: 10
Source: full-release
Hydrated at: 2026-06-01 01:46:14

Label at a glance#

ProductAlcohol

Active ingredientALCOHOL

Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Contacts and useful links#

PhoneLabel contact855-423-2630

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

do not store above 105⁰F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

PROVIDENCE, RI 02908 USA

DSP-TN-21091

DSP-MO-20087

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EQUALINE ^®

MOISTURIZING

Hand Sanitizer

with Vitamin E

32 FL OZ (1 QT) 946 mL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	10
247835	ethanol 0.62 ML/ML Topical Solution	SCD	10
247835	ethanol 62 % Topical Solution	SY	10
247835	ethyl alcohol 62 % Topical Solution	SY	10

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0020397FB		mm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
41163-975-16	Alcohol	59 mL in 1 BOTTLE, PLASTIC	LIQUID	59	10
41163-975-34	Alcohol	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	10
41163-975-45	Alcohol	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	10

Products#

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

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

Alcohol
WATER
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
ISOPROPYL MYRISTATE
TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41163-975	41163-975-16, 41163-975-34, 41163-975-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
TOCOPHEROL	R0ZB2556P8	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
9	2025-11-03	monthly-update	2026-06-03 17:39:49
7	2025-09-16	full-release	2026-06-01 01:13:56

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
Alcohol	ALCOHOL	United Natural Foods, Inc. dba UNFI	ccf505f6-2b34-4a18-af07-92ed505644ff	2026-02-17	Warnings, Adverse reactions	Exact identifier ndc (package): 41163-975-16 ndc (package): 41163-975-45 ndc (package): 41163-975-34 ndc (product): 41163-975 ndc11 (package): 41163097516 ndc11 (package): 41163097534 ndc11 (package): 41163097545 spl id: 4b0952ea-42d6-946f-e063-6394a90a031a spl set id: ccf505f6-2b34-4a18-af07-92ed505644ff

Reported adverse events (FAERS/openFDA)#

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