HAND SANITIZER GEL DRUM

Manufacturer: COMERCIAL GOURA,S. DE R.L.
Effective date: 2020-06-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:16:37

Label at a glance#

ProductPERFECT LIFE

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Directions Place enough product on hands to cover all surfaces. Rub hands together until dry.

Label contents#

Full prescribing information#

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive ingredients Water (Aqua), Glycerin, Carbomer, Triethanolamine

DIRECTIONS

INDICATIONS & USAGE SECTION

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

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.

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredient. Ethyl Alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Purpose Antmicrobial

WARNINGS AND PRECAUTIONS SECTION

Warnings

For external use only. Flammable. Keep away from heat or flame

Children under 6 years of age should be supervised when using.

Other information

Store below 110°F (43°C)

WARNINGS

WARNINGS SECTION

Warnings

For external use only. Flammable. Keep away from heat or flame

STOP USE AND ASK A DOCTOR

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUM LABEL 200 L

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78501-2000-8	2022-01-28	C162847	48780-1	d6a99b39-8e0c-a426-e053-dadaa90af4c2	HAND SANITIZER GEL DRUM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78501-2000-8	PERFECT LIFE	200 L in 1 DRUM	GEL	200		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78501-2000	PERFECT LIFE (ALCOHOL) GEL [COMERCIAL GOURA,S. DE R.L.]	1	Legacy NDC, 1 package rows	20200609_a78a073c-6b0c-201b-e053-2a95a90aa3a6.zip

Products#

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

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

PERFECT LIFE
ALCOHOL
CARBOMER 940
GLYCERIN
TRIETHANOLAMINE CAPROYL GLUTAMATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78501-2000	78501-2000-8

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
CARBOMER 940	4Q93RCW27E	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
TRIETHANOLAMINE CAPROYL GLUTAMATE	0F2FO57253	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
a78a073c-6b0d-201b-e053-2a95a90aa3a6			a78a073c-6b0c-201b-e053-2a95a90aa3a6	2020-06-07	Warnings	Exact identifier spl id: a78a073c-6b0d-201b-e053-2a95a90aa3a6 spl set id: a78a073c-6b0c-201b-e053-2a95a90aa3a6

Reported adverse events (FAERS/openFDA)#

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