Sani T Hand Sanitizer GEL

Manufacturer: Corporativo Cubrete, S.A. de C.V.
Effective date: 2022-01-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:46:19

Label at a glance#

ProductSani T Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially cause disease. For use when soap and water are not available.

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially cause disease.
For use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable

Keek away from fire or flame
For external use only.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, ger medical help in a PoisonControl Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product.

Other information

SPL UNCLASSIFIED SECTION

Store below 110° F (43°C)
May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Triethanolamine, Carbomer, Polysorbate, Water, Glycerin.

Questions?

OTC - QUESTIONS SECTION

+52 1 56 1876 7678 info@cubret.mx

79410-002-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041498	ethanol 80 % Topical Gel	PSN	2
1041498	ethanol 0.8 ML/ML Topical Gel	SCD	2
1041498	ethanol 80 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79410-002-01	2023-07-28	C162847	48780-1	0191ceaa-6121-198a-e063-dbdaa90aec3e	Sani T Hand Sanitizer GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79410-002-01	Sani T Hand Sanitizer	250 mL in 1 BOTTLE	GEL	250		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79410-002	SANI T HAND SANITIZER (ALCOHOL) GEL [CORPORATIVO CUBRETE, S.A. DE C.V.]	2	Legacy NDC, 1 package rows	20220105_ad116efc-68a2-559f-e053-2995a90aeb0f.zip

Products#

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

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

Sani T Hand Sanitizer
ALCOHOL
TROLAMINE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79410-002	79410-002-01

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
TROLAMINE	9O3K93S3TK	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	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
d4c5c2ad-b662-603d-e053-2a95a90a0ef4			ad116efc-68a2-559f-e053-2995a90aeb0f	2022-01-04	Warnings	Exact identifier spl id: d4c5c2ad-b662-603d-e053-2a95a90a0ef4 spl set id: ad116efc-68a2-559f-e053-2995a90aeb0f

Reported adverse events (FAERS/openFDA)#

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