FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Guangdong Boxi High-tech Co.,Ltd.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:57

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin

Dosage and administration

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

Storage and handling

Store below 30 C(86 F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62.0%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin

WARNINGS

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children if swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

Store below 30 C(86 F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Acrylates copolymer, Triethanolamine, Fragrance,Aloe barbadensis leaf extract, Tocopherol, Denatonium benzoate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30ml-280ml30ml-280ml300ml-5000ml300ml-5000ml

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75702-00675702-006-01, 75702-006-02, 75702-006-03, 75702-006-04, 75702-006-05, 75702-006-06, 75702-006-07, 75702-006-08, 75702-006-09, 75702-006-10, 75702-006-11, 75702-006-12, 75702-006-13, 75702-006-14, 75702-006-15, 75702-006-16, 75702-006-17, 75702-006-18, 75702-006-19, 75702-006-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
DENATONIUM BENZOATE4YK5Z54AT2IACT
BENZYL ALCOHOLLKG8494WBHIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOEV5VD430YW9IACT
TROLAMINE9O3K93S3TKIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML · Source PDF

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
b96383b8-f829-2df0-e053-2995a90aa46ea3c7a532-f7b8-52d5-e053-2995a90a0ba62021-01-21WarningsExact identifier
spl set id: a3c7a532-f7b8-52d5-e053-2995a90a0ba6

Reported adverse events (FAERS/openFDA)#

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