WISH RUBBING ALCOHOL 50% Winter Green

Manufacturer
LJ Pharma
Effective date
2026-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:05

Label at a glance#

ProductWISH RUBBING ALCOHOL 50% Winter Green
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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 50%

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 heat or flame.
  • 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 the eyes
  • Do not inhale
  • Do not apply over large areas of the body
  • Do not use longer than one week unless directed by doctor

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.

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.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

FD&C Green #3, FD&C Yellow #5, methyl salicylate, purified water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN1
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD1
616456isopropyl alcohol 50 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-010-01WISH RUBBING ALCOHOL 50% Winter Green12 in 1 CARTONLIQUID121
84809-010-01WISH RUBBING ALCOHOL 50% Winter Green473 mL in 1 BOTTLELIQUID4731
84809-010-02WISH RUBBING ALCOHOL 50% Winter Green946 mL in 1 BOTTLELIQUID9461
84809-010-02WISH RUBBING ALCOHOL 50% Winter Green8 in 1 CARTONLIQUID81

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
84809-01084809-010-01, 84809-010-02

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
WISH RUBBING ALCOHOL 50% Winter GreenISOPROPYL ALCOHOLLJ Pharmafbb45bde-b733-4524-bfa9-ae819ad399732026-01-29WarningsExact identifier
ndc (package): 84809-010-02
ndc (package): 84809-010-01
ndc (product): 84809-010
ndc11 (package): 84809001002
ndc11 (package): 84809001001
spl id: 498b2989-8c8e-d034-e063-6294a90aeaf7
spl set id: fbb45bde-b733-4524-bfa9-ae819ad39973

Reported adverse events (FAERS/openFDA)#

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