WISH 91% ISOPROPYL RUBBING ALCOHOL

Manufacturer
LJ Pharma
Effective date
2025-07-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:42

Label at a glance#

ProductWISH 91% ISOPROPYL RUBBING ALCOHOL
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Indications and uses

First aid to help prevent the risk of infection in minor cuts, Scrapes & Burns.

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 bandag. If bandaged, let dry first

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 91%

Purpose

OTC - PURPOSE SECTION

FIRST AID ANTISEPTIC

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in minor cuts, Scrapes & Burns.

Warnings

WARNINGS SECTION

  • For external use only
  • IF taken internally, Serious gastric disturbances will result.  Flammable ,Keep away from fire or flame, heat, spark, electrical
  • Use only in a well-ventilated area:Fumes may be toxic.

Ask a doctor before use if you havedeep or puncture wounds, Animal bites or serious burns.

When using this product:

  • Do not get in eyes
  • Do not inhale
  • Do not apply over large areas of the body
  • Do not use longer than one week

Stop use and ask doctor ifconditions persist or get worse

Keep out of reach of children In case of ingestion , get medical help or contact a poison. control center right away.

Caution- Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

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 bandag.
  • If bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

  • Does not contain, nor is intended as a substitute for grain or ethyl alchol.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1539800isopropyl alcohol 91 % Topical SprayPSN1
1539800isopropyl alcohol 0.91 ML/ML Topical SpraySCD1
1539800isopropyl alcohol 91 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-006-01WISH 91% ISOPROPYL RUBBING ALCOHOL12 in 1 CARTONLIQUID121
84809-006-01WISH 91% ISOPROPYL RUBBING ALCOHOL296 mL in 1 BOTTLE, SPRAYLIQUID2961

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
84809-00684809-006-01

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
WISH 91% ISOPROPYL RUBBING ALCOHOLISOPROPYL ALCOHOLLJ Pharma449df7ac-97ac-41f3-a3c8-cf0d7c597e052025-07-17WarningsExact identifier
ndc (package): 84809-006-01
ndc (product): 84809-006
ndc11 (package): 84809000601
spl id: 3a247c6d-7356-9af6-e063-6294a90a3dc0
spl set id: 449df7ac-97ac-41f3-a3c8-cf0d7c597e05

Reported adverse events (FAERS/openFDA)#

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