Antibacterial Hand Sanitizer

Manufacturer: Zhejiang Ayan Biotech Co.,Ltd.
Effective date: 2023-11-06
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:59:20

Label at a glance#

ProductAntibacterial Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

• For Hand Sanitizing

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only-hands.

Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands thoroughly with product and allow to dry without wiping. • For children under 6 age use only under adult supervision.

• Not recommended for infants.

Other Information

SPL UNCLASSIFIED SECTION

• Do not store above 105°F. • May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carborner, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water. Yellow 5 (CI 19140), Blue 1 (CI 42090)

Package Labeling: 70412-133-15

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5

Package Labeling: 70412-133-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	3
581660	ethanol 0.62 ML/ML Topical Gel	SCD	3
581660	ethanol 62 % Topical Gel	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70412-133-15	Antibacterial Hand Sanitizer	15 mL in 1 BOTTLE	GEL	15		3
70412-133-30	Antibacterial Hand Sanitizer	30 mL in 1 BOTTLE	GEL	30		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70412-133	ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG AYAN BIOTECH CO.,LTD.]	3	Current NDC, Legacy NDC, 2 package rows	20231108_9c56afa2-c06c-fa03-e053-2995a90a7437.zip

Products#

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

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

Antibacterial Hand Sanitizer
ALCOHOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
TROLAMINE
WATER
FD&C YELLOW NO. 5
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70412-133	70412-133-15, 70412-133-30

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	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
Antibacterial Hand Sanitizer	ALCOHOL	Zhejiang Ayan Biotech Co.,Ltd.	9c56afa2-c06c-fa03-e053-2995a90a7437	2023-11-06	Warnings	Exact identifier ndc (package): 70412-133-30 ndc (package): 70412-133-15 ndc (product): 70412-133 ndc11 (package): 70412013315 ndc11 (package): 70412013330 spl id: 0986d827-1f2d-802d-e063-6394a90aa6b9 spl set id: 9c56afa2-c06c-fa03-e053-2995a90a7437

Reported adverse events (FAERS/openFDA)#

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