Simply U 849.001/849AB-AG,BA

Manufacturer: Nice-Pak Products, LLC
Effective date: 2026-08-18
Label type: HUMAN OTC DRUG LABEL
Version: 54
Source: daily-update
Hydrated at: 2026-08-21 02:01:27

Label at a glance#

ProductAlcohol

Active ingredientALCOHOL

Label structure13 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

Storage and handling

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

Contacts and useful links#

PhoneLabel contact1-888-593-0593

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 exterenal 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Claims

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed By: Nice-Pak Products, LLC

8800 Page Ave.,

St. Louis, MO 63114

1-888-593-0593

Principal panel display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SIMPLY U ^®

Moisturizing

Hand Sanitizer

With Vitamin E

Kills 99.99% of germs*

FORMULA MADE IN USA

EMPLOYEE-OWNED

2 FL OZ (59 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11344-849	11344-849-16, 11344-849-34, 11344-849-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
TOCOPHEROL	R0ZB2556P8	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
53	2026-03-13	full-release	2026-06-01 01:50:14

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	Nice-Pak Products, LLC	dc071394-60de-4b13-a962-9a643b01b106	2026-08-18	Warnings, Adverse reactions	Exact identifier ndc (package): 11344-849-34 ndc (package): 11344-849-16 ndc (package): 11344-849-45 ndc (product): 11344-849 ndc11 (package): 11344084916 ndc11 (package): 11344084945 ndc11 (package): 11344084934 spl id: 5953df05-a352-1b7e-e063-6294a90afc8d spl set id: dc071394-60de-4b13-a962-9a643b01b106

Reported adverse events (FAERS/openFDA)#

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