Tego Systems Professional Grade Hand Sanitizer

Manufacturer: Tego systems Corp
Effective date: 2021-02-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:37:41

Label at a glance#

ProductTego Systems Professional Grade Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Hand Sanitizer to help decrease bacteria on the skin

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin

Warnings

WARNINGS SECTION

External use only-hands

Flammable. Keep away from heat or flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

skin irritation develops.

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

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

Other information

SPL UNCLASSIFIED SECTION

Store below 110°F (43°C)
May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Vitamin E, 1,2-Propanediol, carbomer, triethanolamine, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81497-700-01	2023-01-30	C162847	48780-1	f386c649-a6d8-0266-e053-dadaa90a7c1a	Tego Systems Professional Grade Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81497-700-01	Tego Systems Professional Grade Hand Sanitizer	300 mL in 1 BOTTLE	GEL	300		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81497-700	TEGO SYSTEMS PROFESSIONAL GRADE HAND SANITIZER (ALCOHOL) GEL [TEGO SYSTEMS CORP]	1	Legacy NDC, 1 package rows	20210203_ba5e04e0-75a6-078a-e053-2a95a90ae730.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Tego Systems Professional Grade Hand Sanitizer
ALCOHOL
.ALPHA.-TOCOPHEROL
PROPYLENE GLYCOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81497-700	81497-700-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	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
ba5dfbe5-ad5a-1a18-e053-2a95a90a4f19			ba5e04e0-75a6-078a-e053-2a95a90ae730	2021-02-02	Warnings	Exact identifier spl id: ba5dfbe5-ad5a-1a18-e053-2a95a90a4f19 spl set id: ba5e04e0-75a6-078a-e053-2a95a90ae730

Reported adverse events (FAERS/openFDA)#

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