FDA.reportPublic FDA data

IG SURF 5073 HAND SANITIZER GEL 1000 liter

Manufacturer
India Glycols Limited
Effective date
2020-10-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:10:37

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

  • hand sanitizer to decrease bacteria on the skin
  • recommended for repeated use
  • for use when soap and water not available

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire/flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

do not get into eyes . In case of contact. rinse eyes throughly with water

OTC - STOP USE SECTION

  • irritataion and redness develop
  • condition persist for 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 Poison Control Center right away.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water,glycerine,carbomer,aloe vera,amino methyl propanol, fragrance, hydrogen peroxide, denatonium benzoate, tocopherol, tert-butyl alcohol

DOSAGE & ADMINISTRATION SECTION

Topical Application

Wet hands thoroughly with product and allow to dry without wiping

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000 Literl NDC: 80837-001-10 BackBack FrontFront

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80837-00280837-002-10, 80837-002-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TERT-BUTYL ALCOHOLMD83SFE959IACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT

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
c30326e2-39ec-68c9-e053-2995a90a0aaab1dac821-3044-5d0c-e053-2995a90ac36f2021-05-23WarningsExact identifier
spl set id: b1dac821-3044-5d0c-e053-2995a90ac36f

Reported adverse events (FAERS/openFDA)#

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