WISH- isopropyl alcohol solution

Manufacturer
CLICK PRODUCTS LLC
Effective date
2020-09-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:40

Label at a glance#

ProductWish
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Dosage and administration

Clean the affected area. Apply small amount of this product on the area 1-3 times daily. Let the alcohol dry on skin before using bandages. May be covered with a sterile bandage.

Storage and handling

Store at room temperature Does not contain, nor is intended as a substitute for grain or ethyl alcohol

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (91% conc.)

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

Flammable keep away from fire and flame, heat spark or electricity.
If taken internally, serious gastric disturbances will result.

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

When using this product

  • Do not get in eyes
  • Do not apply over large areas of the body
  • Do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if conditions persist or gets worse.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area.
Apply small amount of this product on the area 1-3 times daily.
Let the alcohol dry on skin before using bandages.
May be covered with a sterile bandage.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature
  • Does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582901isopropyl alcohol 91 % Topical SolutionPSN1
582901isopropyl alcohol 0.91 ML/ML Topical SolutionSCD1
582901isopropyl alcohol 91 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71611-055-012022-01-28C16284748780-1d6a99b39-e1de-a426-e053-dadaa90af4c2WISH- isopropyl alcohol solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71611-055-01Wish500 mL in 1 BOTTLE, PLASTICSOLUTION5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71611-055WISH (ISOPROPYL ALCOHOL) SOLUTION [CLICK PRODUCTS LLC]1Legacy NDC, 1 package rows20200908_aebd3981-366e-204f-e053-2995a90aaf75.zip

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
71611-05571611-055-01

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
aebd4ce3-ffab-5753-e053-2a95a90a046faebd3981-366e-204f-e053-2995a90aaf752020-09-07WarningsExact identifier
spl id: aebd4ce3-ffab-5753-e053-2a95a90a046f
spl set id: aebd3981-366e-204f-e053-2995a90aaf75

Reported adverse events (FAERS/openFDA)#

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