Advanced

Manufacturer: Amazon.Com Services LLC | Nice-Pak Products, LLC
Effective date: 2026-03-09
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:49:21

Label at a glance#

ProductAdvanced

Active ingredientALCOHOL

Label structure15 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 contact1-877-485-0385

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

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

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Questions?

OTC - QUESTIONS SECTION

1-877-485-0385

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by GOJO Industries, Inc., distributor of Purell Advanced Hand Sanitizer.

Claim

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

DSP-TN-21091 DSP-MO-20087

Made in USA with US and foreign components.

DISTRIBUTED BY: AMAZON.COM SERVICES LLC

Seattle, WA 98109

PLASTIC BOTTLE

Do Not Recycle

how2recycle.info

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

amazon basics

Compare to Purell ^®Advanced Hand Sanitizer*

NDC 72288-370-45

Hand Sanitizer

Moisturizing

Kills more than 99.99% of germs**

32 FL OZ (1 QT) 946 mL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	7
581662	ethanol 0.7 ML/ML Topical Gel	SCD	7
581662	ethanol 70 % Topical Gel	SY	7
581662	ethyl alcohol 70 % Topical Gel	SY	7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72288-370-45	Advanced	946 mL in 1 BOTTLE, PUMP	GEL	946		7
72288-370-88	Advanced	1890 mL in 1 BOTTLE, PUMP	GEL	1890		7

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Advanced
Ethyl Alcohol
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)
SULISOBENZONE
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72288-370	72288-370-45, 72288-370-88

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERYL CAPRYLATE/CAPRATE	G7515SW10N	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)	71DD5V995L	IACT
SULISOBENZONE	1W6L629B4K	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
6	2026-02-06	monthly-update	2026-06-03 17:56:16

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
Advanced	ETHYL ALCOHOL	Amazon.Com Services LLC	f5722d72-96b5-4aea-a67a-68aeefb63203	2026-03-09	Warnings, Adverse reactions	Exact identifier ndc (package): 72288-370-45 ndc (package): 72288-370-88 ndc (product): 72288-370 ndc11 (package): 72288037088 ndc11 (package): 72288037045 spl id: 4c9beca6-19c5-e78b-e063-6294a90a864d spl set id: f5722d72-96b5-4aea-a67a-68aeefb63203

Reported adverse events (FAERS/openFDA)#

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