FDA.reportPublic FDA data

DefendMax Sanitizing Wipes

Manufacturer
Etailer Limited
Effective date
2020-11-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:04:36

Label at a glance#

ProductDefendMax Sanitizing Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Apply to Hands Wet hands thoroughly with product and allow to dry without wiping.

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

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use(s)

INDICATIONS & USAGE SECTION

Decreases bacteria on 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
  • if you are allergic to any of the ingredients

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. These may be signs of a serious condition.

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

  • Apply to Hands
  • Wet hands thoroughly with product and allow to dry without wiping.

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

Benzalkonium Chloride, Chlorhexidine Diacetate, Nano Silver Ions (Ag+), Vitamin E, Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1ct (78256-100-00), 100ct box (78256-100-10)

wipeswipes

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
78256-10078256-100-00, 78256-100-10

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
ALPHA-TOCOPHEROLH4N855PNZ1IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
SILVER CATION57N7B0K90AIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CHLORHEXIDINE ACETATE5908ZUF22YIACT

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
b55fc5ed-b568-f9c4-e053-2a95a90ab59ba7d5d667-e887-60cf-e053-2995a90a26eb2020-11-30WarningsExact identifier
spl id: b55fc5ed-b568-f9c4-e053-2a95a90ab59b
spl set id: a7d5d667-e887-60cf-e053-2995a90a26eb

Reported adverse events (FAERS/openFDA)#

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