TECOT SANITIZER

Manufacturer: TECOT Co.,Ltd. | Kukbo Science Co., Ltd.
Effective date: 2020-06-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:15:36

Label at a glance#

ProductTECOT SANITIZER

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

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

Dosage and administration

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry. • Supervise children in the use of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% v/v

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Benzalkonium chloride, Glycerin, Carbomer, Trolamine, Aloe extract, Flavor

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame
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Do not use
• in children less than 2 months of age
• on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Uses

INDICATIONS & USAGE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
• Supervise children in the use of this product.

Other information

OTHER SAFETY INFORMATION

• Store between 15℃ to 30℃ (59℉ to 86℉)
• Avoid freezing and excessive heat above 40℃ (104℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

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

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	8806049601411	GTIN-13: 8806049601411 EAN-13: 8806049601411 GTIN storage (14 digits): 08806049601411	500 bottle.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78452-010-01	2021-07-23	C162847	48780-1	c7ccaba7-2613-fd44-e053-dadaa90aa01b	a40bee0c-25b6-4ea7-8292-d51780319d59

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78452-010-01	TECOT SANITIZER	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78452-010	TECOT SANITIZER (ALCOHOL) GEL [TECOT CO.,LTD.]	1	Legacy NDC, 1 package rows	20200602_a40bee0c-25b6-4ea7-8292-d51780319d59.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

TECOT SANITIZER
ALCOHOL
Water
Benzalkonium chloride
Glycerin
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
ALOE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78452-010	78452-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
Benzalkonium chloride	F5UM2KM3W7	IACT
Glycerin	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
ALOE	V5VD430YW9	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
98f73035-01e3-46a8-9883-23fcb8e2a91f			a40bee0c-25b6-4ea7-8292-d51780319d59	2020-06-02	Warnings	Exact identifier spl id: 98f73035-01e3-46a8-9883-23fcb8e2a91f spl set id: a40bee0c-25b6-4ea7-8292-d51780319d59

Reported adverse events (FAERS/openFDA)#

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