Purox Hand Sanitizer

Manufacturer: Purox
Effective date: 2020-07-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:21:29

Label at a glance#

ProductPurox Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly spread on both hands and rub into th skin until dry. Children under 6 years old should be supervised when using this product.

Storage and handling

store between 106F (41C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 85% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame

For external use only

OTC - WHEN USING SECTION

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly spread on both hands and rub into th skin until dry.
Children under 6 years old should be supervised when using this product.

Other information:

STORAGE AND HANDLING SECTION

store between 106F (41C)
may discolor certain fabrics or surfaces

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Deionized Water, Aloe, Triethanolamine, Carbomer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041851	ethanol 85 % Topical Gel	PSN	1
1041851	ethanol 0.85 ML/ML Topical Gel	SCD	1
1041851	ethanol 85 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78186-001-02	2022-01-28	C162847	48780-1	d6a99b39-f81d-a426-e053-dadaa90af4c2	33267621-bbf0-45a5-96f8-ee37e011619e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78186-001-02	Purox Hand Sanitizer	0.384 L in 1 BOTTLE	GEL	0.384		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78186-001	PUROX HAND SANITIZER (ALCOHOL) GEL [PUROX]	1	Legacy NDC, 1 package rows	20200716_33267621-bbf0-45a5-96f8-ee37e011619e.zip

Products#

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

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

Purox Hand Sanitizer
Alcohol
ALOE
TROLAMINE
POLYACRYLIC ACID (250000 MW)
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78186-001	78186-001-02

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
ALCOHOL	3K9958V90M	ACTIB
ALOE	V5VD430YW9	IACT
TROLAMINE	9O3K93S3TK	IACT
POLYACRYLIC ACID (250000 MW)	9G2MAD7J6W	IACT
WATER	059QF0KO0R	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
5d28e145-0489-4c5b-b319-231ad312a551			33267621-bbf0-45a5-96f8-ee37e011619e	2020-07-08	Warnings	Exact identifier spl id: 5d28e145-0489-4c5b-b319-231ad312a551 spl set id: 33267621-bbf0-45a5-96f8-ee37e011619e

Reported adverse events (FAERS/openFDA)#

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