FDA.reportPublic FDA data

Isopropyl Alcohol 70 Pad

Manufacturer
Winner Medical (Jiayu) Co., Ltd.
Effective date
2021-10-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:31:42

Label at a glance#

ProductIsopropyl Alcohol 70 Pad
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

for preparation of the skin prior to an injection first aid to help decrease the risk of bacteria contamination in minor cuts, scrapes

Dosage and administration

Patient Preoperative Skin Preparation Clean the area Dry and repeat procedure First Aid Antiseptic Clean the affected area Apply a small amount of this product on the area 1 to 3 times daily Maybe covered with a sterile bandage If bandaged, let dry first

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Patient Preoperative Skin Preparation First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for preparation of the skin prior to an injection
  • first aid to help decrease the risk of bacteria contamination in minor cuts, scrapes

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame

For external use only

Do not use 

OTC - DO NOT USE SECTION

  • with electrocautery procedures
  • in the eyes or apply over large areas of the body
  • longer that 1 week unless directed by a doctor 

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • the condtion persists for more than 72 hours
  • the condition gets worse

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Centre right away

Directions

DOSAGE & ADMINISTRATION SECTION

Patient Preoperative Skin Preparation

  • Clean the area
  • Dry and repeat procedure

First Aid Antiseptic

  • Clean the affected area
  • Apply a small amount of this product on the area 1 to 3 times daily
  • Maybe covered with a sterile bandage
  • If bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

store in a cool, dry place

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water

Package Labeling:50ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:100ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:200ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

Package Labeling:400ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4Bottle4

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71870-00571870-005-01, 71870-005-02, 71870-005-03, 71870-005-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
cea404b9-eb18-d35b-e053-2995a90a5b454b78ab42-3a5e-4b33-bef8-47acaa0978072021-10-18WarningsExact identifier
spl id: cea404b9-eb18-d35b-e053-2995a90a5b45
spl set id: 4b78ab42-3a5e-4b33-bef8-47acaa097807

Reported adverse events (FAERS/openFDA)#

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