DailyGard Wipes 75 Percent Ethyl Alcohol

Manufacturer
YMF Carpets, Inc
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:19:28

Label at a glance#

ProductDailyGard Wipes 75 Percent Ethyl Alcohol
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

-Wipe hands, discard properly in trash receptacle. -Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

75% Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use[s]:

INDICATIONS & USAGE SECTION

For hand sanitizing that helps reduce bacteria on the skin, recommended for repeated use.

Warning

WARNINGS SECTION

For external use only-Highly Flammable-Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

-On open skin wounds

When using this product:

OTC - WHEN USING SECTION

-Avoid contact with eyes, ears, and mouth. In case of contact with eyes, flush with water.

-Avoid contact with broken skin.Do not inhale or ingest.

Stop use and ask a doctor

OTC - STOP USE SECTION

if skin irritation or rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, contact a Poison Control Center or a doctor.

Directions:

DOSAGE & ADMINISTRATION SECTION

-Wipe hands, discard properly in trash receptacle.

-Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information:

SPL UNCLASSIFIED SECTION

-Store at room temperature. Do not store above 105°F.

-Do not freeze.

-May disolor some fabrics. Harmful to wood finishes and plastics.

-Effective at eliminating more than 99.9% of many common harmful germs and bacteria in as little as 15 seconds.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe barbadensis leaf juice, Tocopheryl acetate

Package Labeling:50 count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:100 count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78198-00478198-004-01, 78198-004-02

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
f44ad347-164e-1c91-e053-2a95a90a82223472734b-e1f6-4c36-835a-da707ff893c32023-02-09WarningsExact identifier
spl set id: 3472734b-e1f6-4c36-835a-da707ff893c3

Reported adverse events (FAERS/openFDA)#

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