Alcohol wipes

Manufacturer
Anhui Germaphob Daily Commodity Co., Ltd.
Effective date
2021-02-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:51:07

Label at a glance#

ProductAlcohol wipes
Active ingredientALCOHOL
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

Ethyl Alcohol75%

Purpose

OTC - PURPOSE SECTION

Antibacterial

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

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

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

/

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, Aloe barbadensis leaf juice, Tocopheryl acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80110-012-01 100P80110-012-01 100P

Products#

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DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80110-01280110-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
d4d2b656-9a37-4c3a-e053-2a95a90abff4ae61a16a-50aa-9c59-e053-2995a90a47042022-01-05WarningsExact identifier
spl set id: ae61a16a-50aa-9c59-e053-2995a90a4704

Reported adverse events (FAERS/openFDA)#

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