FDA.reportPublic FDA data

WISH RUBBING ALCOHOL 70% WINTERGREEN

Manufacturer
LJ Pharma
Effective date
2025-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:10

Label at a glance#

ProductWISH RUBBING ALCOHOL 70% WINTERGREEN
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 70%

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.
  • Use only in a well-ventilated area:Fumes may be toxic.

Ask a doctor before use if you have deepor 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 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

Purified Water , Methyl Salicylate , FD&C GREEN #3, FD&C Yellow #5

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN1
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD1
808520isopropyl alcohol 70 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-003-01WISH RUBBING ALCOHOL 70% WINTERGREEN12 in 1 CARTONLIQUID121
84809-003-01WISH RUBBING ALCOHOL 70% WINTERGREEN355 mL in 1 BOTTLELIQUID3551
84809-003-02WISH RUBBING ALCOHOL 70% WINTERGREEN12 in 1 CARTONLIQUID121
84809-003-02WISH RUBBING ALCOHOL 70% WINTERGREEN473 mL in 1 BOTTLELIQUID4731
84809-003-03WISH RUBBING ALCOHOL 70% WINTERGREEN946 mL in 1 BOTTLELIQUID9461
84809-003-03WISH RUBBING ALCOHOL 70% WINTERGREEN12 in 1 CARTONLIQUID121

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
84809-00384809-003-01, 84809-003-02, 84809-003-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
METHYL SALICYLATELAV5U5022YIACT
FD&C GREEN NO. 33P3ONR6O1SIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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 RUBBING ALCOHOL 70% WINTERGREENISOPROPYL ALCOHOLLJ Pharma98ebf7a7-7c13-4feb-90b5-21cc6dab99f62025-06-16WarningsExact identifier
ndc (package): 84809-003-03
ndc (package): 84809-003-02
ndc (package): 84809-003-01
ndc (product): 84809-003
ndc11 (package): 84809000303
ndc11 (package): 84809000301
ndc11 (package): 84809000302
spl id: 37b15d3e-e088-f8ae-e063-6394a90aec43
spl set id: 98ebf7a7-7c13-4feb-90b5-21cc6dab99f6

Reported adverse events (FAERS/openFDA)#

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