Isopropyl Alcohol Wipes

Manufacturer
Xiamen Yiukin Paper Products Co.,ltd
Effective date
2021-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:19:49

Label at a glance#

ProductIsopropyl Alcohol Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Tear along the edge and take out the wipe. Thoroughly clean hands or affected area. Recommended for single use. Do not flush after using. Please throw the wipe in the trash.

Storage and handling

Store at room temperature Avoid sunlight irradiating.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 75% Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the ingredients

OTC - STOP USE SECTION

Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or consult a Poison Control Center immediately.

Directions Of Use

DOSAGE & ADMINISTRATION SECTION

  • Tear along the edge and take out the wipe. Thoroughly clean hands or affected area.
  • Recommended for single use.
  • Do not flush after using. Please throw the wipe in the trash.

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature
  • Avoid sunlight irradiating.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, Cetylpyridinium chloride, Chlorphenesin, Propylene glycol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AMC

Safe & Clean

Hand Wipes 75% Isopropyl Alcohol

PDPPDP

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79288-01979288-019-01

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
ddee9ab7-7f1a-bd09-e053-2995a90a8358b3899c79-4d98-5e60-e053-2995a90a2e4f2022-05-01WarningsExact identifier
spl set id: b3899c79-4d98-5e60-e053-2995a90a2e4f

Reported adverse events (FAERS/openFDA)#

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