FDA.reportPublic FDA data

INSTANT HAND SANITIZER

Manufacturer
SINGWONG ASIA PACIFIC (BOLUO) CO., LTD.
Effective date
2020-09-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 23:16:15

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Put enough product in your palm to cover skin and rub hands together briskly until dry Children under 6 years of age should be supervised when using HY

Storage and handling

Store below 110F/43C May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Anfimicrobial

Purpose

OTC - PURPOSE SECTION

Purpose: Anfimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

flammable.keep away from fire or flame.

Keen away fom fire or flame

For extemal use only

When using this product do not use near the eyes.

In case of contact rinse eyes thoroughly with water

-Stop use and ask a doctor if imitation orrash appears and lasts.

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

Do not use

OTC - DO NOT USE SECTION

When using this produc do not use near the eves.

OTC - WHEN USING SECTION

When using this produc do not use near the eyes.

In case of contact rinse eyes thoroughly with water

OTC - STOP USE SECTION

-Stop use and ask a doctor if imitation orrash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover skin and rub hands together briskly until dry

Children under 6 years of age should be supervised when using HY

Other information

STORAGE AND HANDLING SECTION

  • Store below 110F/43C
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water,glycerin,aloe barbadensis leaf extract,acrylates/C10-30 alkyl acrylate crosspolymer,triethanolamine.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75283-007-0175283-007-0175283-007-0275283-007-0275283-007-0375283-007-0375283-007-0475283-007-0475283-007-0575283-007-0575283-007-0675283-007-0675283-007-0775283-007-0775283-007-0875283-007-08

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
75283-00775283-007-01, 75283-007-02, 75283-007-03, 75283-007-04, 75283-007-05, 75283-007-06, 75283-007-07, 75283-007-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CUPRIC TRIETHANOLAMINE6NU949U74EIACT

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
b8d69517-1f45-0e02-e053-2995a90a62e0a341bfc6-e76a-cff7-e053-2a95a90af3282021-01-14WarningsExact identifier
spl set id: a341bfc6-e76a-cff7-e053-2a95a90af328

Reported adverse events (FAERS/openFDA)#

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