FDA.reportPublic FDA data

Instant Hand Sanitizer Gel

Manufacturer
SURYA MAS DAILY CHEMICAL(TIANJIN)CO., LTD.
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:39

Label at a glance#

ProductInstant Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Directions Put enough product in your palm to cover handsand rub hands together briskly until dry. Childrenunder 6 year of age should be supervised whenusing BAGUS

Storage and handling

Store below 110"(43 C)May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%v/v Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Warnings

WARNINGS SECTION

Flammable. Keep away from fire orflame For external use only

Do not use

OTC - DO NOT USE SECTION

  • on open skin wounds

OTC - WHEN USING SECTION

When using this product do not use in or nearthe eyes. In case of contact, rinse eyes thoroughlywith water.

OTC - STOP USE SECTION

Stop use and ask a doctor if imitation or rashappears 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 Cente rright away

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Put enough product in your palm to cover handsand rub hands together briskly until dry. Childrenunder 6 year of age should be supervised whenusing BAGUS

Other information

STORAGE AND HANDLING SECTION

  • Store below 110"(43 C)May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Thickener, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

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
74755-00874755-008-01, 74755-008-02, 74755-008-03

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
NONOXYNOL-2060ZT1XYO5NIACT
POLYOXYL 35 CASTOR OIL6D4M1DAL6OIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b8d74b1c-ad34-3c41-e053-2a95a90a9827a38aa6e5-0d7e-ff6a-e053-2a95a90a27f22021-01-14WarningsExact identifier
spl set id: a38aa6e5-0d7e-ff6a-e053-2a95a90a27f2

Reported adverse events (FAERS/openFDA)#

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