HAND SANITIZER

Manufacturer: Xiamen Tesimeier Biotechnology Co., Ltd.
Effective date: 2020-06-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:57

Label at a glance#

ProductHAND SANITIZER

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping, for children under 6, use only under adult supervision not recommended for infants

Storage and handling

do not store above 41 C(106 F) may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

OTC - WHEN USING SECTION

When using this product
keep out of eyes
In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin
do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

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. Keep sealed when not in use

Directions

DOSAGE & ADMINISTRATION SECTION

wet 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

STORAGE AND HANDLING SECTION

do not store above 41 C(106 F) may discolor some fabrics harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water(aqua), glycerin, carbomer, triethanolamine, peg-40 hydrogenated castor oil, fragrance(parfum), aloe barbadensis leaf extract, tocopheryl acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3025030050100500

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
75606-001-01	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER
75606-001-02	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER
75606-001-03	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER
75606-001-04	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER
75606-001-05	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER
75606-001-06	2022-01-28	C162847	48780-1	d6a99b39-a944-a426-e053-dadaa90af4c2	HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75606-001-01	HAND SANITIZER	30 mL in 1 BOTTLE	GEL	30	1
75606-001-02	HAND SANITIZER	50 mL in 1 BOTTLE	GEL	50	1
75606-001-03	HAND SANITIZER	100 mL in 1 BOTTLE	GEL	100	1
75606-001-04	HAND SANITIZER	250 mL in 1 BOTTLE	GEL	250	1
75606-001-05	HAND SANITIZER	300 mL in 1 BOTTLE	GEL	300	1
75606-001-06	HAND SANITIZER	500 mL in 1 BOTTLE	GEL	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75606-001	HAND SANITIZER GEL [XIAMEN TESIMEIER BIOTECHNOLOGY CO., LTD.]	1	Legacy NDC, 6 package rows	20200617_a830f7de-7982-7c99-e053-2a95a90aa6cb.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

HAND SANITIZER
GLYCERIN
CARBOMER 1342
WATER
ALCOHOL
TROLAMINE
FRAGRANCE LAVENDER & CHIA F-153480
ALOE VERA LEAF
POLYOXYL 40 HYDROGENATED CASTOR OIL
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75606-001	75606-001-01, 75606-001-02, 75606-001-03, 75606-001-04, 75606-001-05, 75606-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER 1342	809Y72KV36	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
TROLAMINE	9O3K93S3TK	IACT
FRAGRANCE LAVENDER & CHIA F-153480	SXS9CO2TZK	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	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
a830f7de-7974-7c99-e053-2a95a90aa6cb			a830f7de-7982-7c99-e053-2a95a90aa6cb	2020-06-16	Warnings	Exact identifier spl id: a830f7de-7974-7c99-e053-2a95a90aa6cb spl set id: a830f7de-7982-7c99-e053-2a95a90aa6cb

Reported adverse events (FAERS/openFDA)#

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