FDA.reportPublic FDA data

Hand and Surface Anti Bacterial Wipes

Manufacturer
VANILLA SUGAR PTY LTD
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:13:18

Label at a glance#

ProductHand and Surface Anti Bacterial Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Peel label and remove wipe. Wipe over hands or surface for 1 minute and allow to dry. Discard wipe after use. Supervise children under 6 years of age when using this product.

Storage and handling

Do not store above 104F°(40°C) May discolour some fabrics or surfaces. Re-seal package to ensure wipes do not dry out. Do not flush wipe down the toilet.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For Hand Sanitizing.
  • To help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

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

  • Peel label and remove wipe.
  • Wipe over hands or surface for 1 minute and allow to dry.
  • Discard wipe after use.
  • Supervise children under 6 years of age when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 104F°(40°C)
  • May discolour some fabrics or surfaces.
  • Re-seal package to ensure wipes do not dry out.
  • Do not flush wipe down the toilet.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10Wipes NDC: 74443-030-01

NDC 74443-030-01NDC 74443-030-01

50Wipes NDC: 74443-030-05

NDC 74443-030-05NDC 74443-030-05

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74443-03074443-030-05, 74443-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
d5fe79da-8e3e-59b8-e053-2995a90ac115a6840cee-74a8-ec20-e053-2995a90ae3ce2022-01-20WarningsExact identifier
spl id: d5fe79da-8e3e-59b8-e053-2995a90ac115
spl set id: a6840cee-74a8-ec20-e053-2995a90ae3ce

Reported adverse events (FAERS/openFDA)#

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