FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Ningbo Pretty Tourism Manufacture Co., ltd
Effective date
2020-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:25

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoroughly with product briskly rub hands together until dry supervise children under 6 years in the use of this product.

Storage and handling

store at 20°C to 25°C (68°F to 77°F) may discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75.0%V/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin.
recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.
Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of contact, rinse eyes thoroughly with wafer.

OTC - WHEN USING SECTION

For external use only.
Flammable, keep away from heat and flame.

Do not use in the eyes. In case of contact, rinse eyes thoroughly with wafer.

OTC - STOP USE SECTION

Stop use, and ask a doctor if irritation and redness develop and persistfor 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 Posion Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product briskly rub hands together until dry supervise children under 6 years in the use of this product.

Other information

STORAGE AND HANDLING SECTION

store at 20°C to 25°C (68°F to 77°F)
may discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aloe vera, Triethanolamine, Vitamin E

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5959

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75749-03675749-036-01

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
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
d39faafd-ea33-dcfa-e053-2a95a90a64ada647e5ee-c379-626b-e053-2995a90aa76d2021-12-20WarningsExact identifier
spl set id: a647e5ee-c379-626b-e053-2995a90aa76d

Reported adverse events (FAERS/openFDA)#

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