FDA.reportPublic FDA data

Hand sanitizer

Manufacturer
FLTR, INC. | Huizhou Baozi Biotechnology Co., Ltd.
Effective date
2020-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:12:10

Label at a glance#

ProductHand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin

Dosage and administration

Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 106°F (41°C) May discolor certain fabrics or suriaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Eohyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.
Harmful if swallowed.
For external use only.
CONTINUED NEXT PAGE

OTC - DO NOT USE SECTION

Do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

Keep out of reach of children . If swallowed, get medkal help or contact Poison Control Center right away.

Do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask aoctor if irritatioin or rash appears and lasts.

OTC - STOP USE SECTION

Stop use and ask aoctor if irritatioin or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children . If swallowed, get medkal help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry

Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

Store below 106°F (41°C)
May discolor certain fabrics or suriaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, caroomer, triethanolamine, fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

90081-009-01 50ml90081-009-01 50ml

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90081-00990081-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b966b068-e3ae-703e-e053-2a95a90a153cb1762c42-ff27-7b2f-e053-2a95a90a24cd2021-01-21WarningsExact identifier
spl set id: b1762c42-ff27-7b2f-e053-2a95a90a24cd

Reported adverse events (FAERS/openFDA)#

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