FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Ningbo Pretty Tourism Manufacture Co., ltd
Effective date
2020-06-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:56

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Apply as needed into palm of hand and thoroughly spreadon both hands, rub until dry. Supervise children under 6 years of age when using this product.

Storage and handling

Store between 15-30 C(59-86°F） Avoid freezing and excessive heat above 40°C(104°F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

on infants
on open skin wounds

OTC - WHEN USING SECTION

When using this product keed out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with Water.

OTC - STOP USE SECTION

Stop use and ask a doctor lf irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply as needed into palm of hand and thoroughly spreadon both hands, rub until dry.
Supervise children under 6 years of age when using this product.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30 C(59-86°F）
Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua). Triethanolamine, Carbomer. Aloe Barbadensis(Aloe Vera)Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate(Vitamin E)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75749-03875749-038-01, 75749-038-02, 75749-038-03, 75749-038-04

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
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d39fab18-68dc-b42b-e053-2995a90a354ca7f75bb4-2900-6aca-e053-2a95a90a01412021-12-20WarningsExact identifier
spl set id: a7f75bb4-2900-6aca-e053-2a95a90a0141

Reported adverse events (FAERS/openFDA)#

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