FDA.reportPublic FDA data

Antibacterial Hand Wipes

Manufacturer
QUEST USA CORP
Effective date
2020-07-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:22:44

Label at a glance#

ProductAntibacterial Hand Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

peel the sticker when you use it. Easily get one wipe at a time. After application, please re-seal the opening sticker firmly to prevent wipes from drying out

Storage and handling

Store between 0-40C (32-104F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For Hand Sanitizer to decrease bacterial on the skin

Warnings

WARNINGS SECTION

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

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 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

peel the sticker when you use it.

Easily get one wipe at a time.

After application, please re-seal the opening sticker firmly to prevent wipes from drying out

Other information

STORAGE AND HANDLING SECTION

  • Store between 0-40C (32-104F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

pure water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 wipes in 1 bag. NDC: 78691-001-01;

100pcs100pcs

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78691-018-022022-12-28C16284748780-1c7ccaba7-1539-fd44-e053-dadaa90aa01bBiopure Antibacterial Hand Wipes
78691-018-022021-07-23C16284748780-1c7ccaba7-1539-fd44-e053-dadaa90aa01bBiopure Antibacterial Hand Wipes

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-01878691-018-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
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
f0e46dec-2e4c-9447-e053-2a95a90a2ea3a7ca7d94-d72b-5623-e053-2a95a90a4df82022-12-28WarningsExact identifier
spl set id: a7ca7d94-d72b-5623-e053-2a95a90a4df8

Reported adverse events (FAERS/openFDA)#

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