Rubbing Alcohol

Manufacturer
Super Dope Laboratories LLC
Effective date
2020-08-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:25:06

Label at a glance#

ProductRubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Dosage and administration

Directions • Clean affected area • Apply a small amount of this product 1-3 times daily • If bandaged let dry first • May be covered with a sterile bandage

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 99% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For first aid use to decrease germs in minor cuts and scrapes

Warnings

WARNINGS SECTION

For external use only.
•If taken internally serious gastric disturbances will result
• Do not use in or near the eyes
• In case of deep or puncture wounds, consult your doctor.
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 have deep or puncture wounds, animal
bites or serious burns.

OTC - WHEN USING SECTION

When using this product
• Do not get into eyes
• Do not apply over large areas of the body
• Do not use longer than one week unless directed by a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if condition persists 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Directions • Clean affected area • Apply a small amount of this product
    1-3 times daily • If bandaged let dry first • May be covered with a sterile
    bandage

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Purified Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3785mL NDC: 74220-006-01

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
402481isopropyl alcohol 99 % Topical SolutionPSN2
402481isopropyl alcohol 0.99 ML/ML Topical SolutionSCD2
402481isopropyl alcohol 99 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74220-006-012022-01-28C16284748780-1d6a99b39-78e2-a426-e053-dadaa90af4c2Super Dope Rubbing Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74220-006-01Rubbing Alcohol3785 mL in 1 BOTTLESOLUTION37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74220-006RUBBING ALCOHOL (ISOPROPYL ALCOHOL) SOLUTION [SUPER DOPE LABORATORIES LLC]2Legacy NDC, 1 package rows20200819_ad186538-5ca1-70ba-e053-2995a90a582f.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
74220-00674220-006-01

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
ad1865f5-9407-eaa4-e053-2995a90aa079ad186538-5ca1-70ba-e053-2995a90a582f2020-08-17WarningsExact identifier
spl id: ad1865f5-9407-eaa4-e053-2995a90aa079
spl set id: ad186538-5ca1-70ba-e053-2995a90a582f

Reported adverse events (FAERS/openFDA)#

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