FDA.reportPublic FDA data

Wet Wipes

Manufacturer
Anhui Germaphob Daily Commodity Co., Ltd.
Effective date
2021-02-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:51:07

Label at a glance#

ProductWet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use in the eyes

Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes

OTC - WHEN USING SECTION

When using this product Stop use and ask a doctor if
irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if
irritation and redness develop
condition persists 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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, EDTA disodium salt, phenoxyethanol, aloe vera leaf juice, tocopheryl acetate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BAG80110-018-03 20PBAG80110-018-03 20PBAG80110-018-01 1PBAG80110-018-01 1PDRUM80110-018-20 800PDRUM80110-018-20 800PDRUM80110-018-10 60P1DRUM80110-018-10 60P1BAG80110-018-02 10PBAG80110-018-02 10PBAG80110-018-06 80PBAG80110-018-06 80PBAG80110-018-04 40PBAG80110-018-04 40PBAG80110-018-08 120PBAG80110-018-08 120PDRUM80110-018-09 40PDRUM80110-018-09 40PDRUM80110-018-11 80PDRUM80110-018-11 80PDRUM80110-018-18 400PDRUM80110-018-18 400PDRUM80110-018-13 120PDRUM80110-018-13 120PBAG80110-018-05 50PBAG80110-018-05 50PDRUM80110-018-19 600PDRUM80110-018-19 600PDRUM80110-018-14 160PDRUM80110-018-14 160PDRUM80110-018-17 260PDRUM80110-018-17 260PDRUM80110-018-16 250PDRUM80110-018-16 250PDRUM80110-018-12 100PDRUM80110-018-12 100PBAG80110-018-07 100PBAG80110-018-07 100PDRUM80110-018-15 200PDRUM80110-018-15 200P

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80110-01880110-018-01, 80110-018-07, 80110-018-04, 80110-018-05, 80110-018-08, 80110-018-06, 80110-018-02, 80110-018-03, 80110-018-09, 80110-018-15, 80110-018-16, 80110-018-17, 80110-018-18, 80110-018-10, 80110-018-19, 80110-018-11, 80110-018-14, 80110-018-12, 80110-018-20, 80110-018-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
EDETATE DISODIUM7FLD91C86KIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
d4d2b928-3e34-1142-e053-2a95a90ad507b201524e-055e-15d3-e053-2a95a90ad7122022-01-05WarningsExact identifier
spl set id: b201524e-055e-15d3-e053-2a95a90ad712

Reported adverse events (FAERS/openFDA)#

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