Preatorian Hand Sanitizer

Manufacturer: Sistema Corporativo Deutzia, S.A. de C.V.
Effective date: 2020-09-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:28:53

Label at a glance#

ProductPreatorian Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

We hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Anticeptic

USES.

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

WARNING

WARNINGS SECTION

For external use only: HANDS. Flammable, keep away from fire or flame.

When using this product:

OTC - WHEN USING SECTION

keep out eyes, in case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. don´t inhale or ingest.

Stop use and ask of 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

We 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

Don´t store above 105°F. may discolor some fabrics. harmful to wood finishes and plastics

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Alkylating, Agent, Aloe.

Package Labeling:125ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2

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
80455-000-01	2022-01-28	C162847	48780-1	d6a99b39-616e-a426-e053-dadaa90af4c2	Preatorian Hand Sanitizer
80455-000-02	2022-01-28	C162847	48780-1	d6a99b39-616e-a426-e053-dadaa90af4c2	Preatorian Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80455-000-01	Preatorian Hand Sanitizer	125 mL in 1 BOTTLE	GEL	125		1
80455-000-02	Preatorian Hand Sanitizer	250 mL in 1 BOTTLE	GEL	250		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80455-000	PREATORIAN HAND SANITIZER (ALCOHOL) GEL [SISTEMA CORPORATIVO DEUTZIA, S.A. DE C.V.]	1	Legacy NDC, 2 package rows	20200910_aee28fa6-02d8-7756-e053-2a95a90aac50.zip

Products#

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

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

Preatorian Hand Sanitizer
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80455-000	80455-000-01, 80455-000-02

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
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB

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
aee279c1-ce57-4f35-e053-2995a90aeaac			aee28fa6-02d8-7756-e053-2a95a90aac50	2020-09-09	Warnings	Exact identifier spl id: aee279c1-ce57-4f35-e053-2995a90aeaac spl set id: aee28fa6-02d8-7756-e053-2a95a90aac50

Reported adverse events (FAERS/openFDA)#

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