Pharmacys Prescription Rubbing Alcohol

Manufacturer
American Consumer Products Corp
Effective date
2020-07-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:19:56

Label at a glance#

ProductPharmacys Prescription Rubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Indications and uses

Uses ● helps reduce bacteria and germs on skin. ● helps relieve minor muscular aches due to exertion.

Dosage and administration

Directions ●clean skin and apply a small amount of this product 1-3 times daily on a selected area as needed ● allow product to remain on skin surface until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (by volume)

Isopropyl alcohol (50% conc.)

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses
● helps reduce bacteria and germs on skin.
● helps relieve minor muscular aches due to exertion.

Warnings

WARNINGS SECTION

Warnings


For external use only


● flammable, keep away from fire or flame


● not recommended for deep puncture wounds, animal bites or serious burns


● if taken internally, serious gastric disturbances will result

When using this product

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.

Stop use

OTC - STOP USE SECTION

Stop use if ● condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Do not use on children less than 2 months of age.
Supervise use in children under 6 years of age to prevent accidental swallowing.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions ●clean skin and apply a small amount of this product 1-3 times daily on a selected area as needed ● allow product to remain on skin surface until dry

Inactive ingredient

INACTIVE INGREDIENT SECTION

Inactive ingredient: purified water (Aqua)

Pharmacys Prescription Isopropyl Rubbing Alcohol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pharmacys Prescription Isopropyl AlcoholPharmacys Prescription Isopropyl Alcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616456isopropyl alcohol 50 % Topical SolutionPSN2
616456isopropyl alcohol 0.5 ML/ML Topical SolutionSCD2
616456isopropyl alcohol 50 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-030-112022-01-28C16284748780-1d6a99b39-5c00-a426-e053-dadaa90af4c2Pharmacys Prescription Rubbing Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-030-11Pharmacys Prescription Rubbing Alcohol350 mL in 1 BOTTLELIQUID3502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-030PHARMACYS PRESCRIPTION RUBBING ALCOHOL (ALCOHOL) LIQUID [AMERICAN CONSUMER PRODUCTS CORP]2Legacy NDC, 1 package rows20200703_a71dedda-b66e-b710-e053-2995a90ac660.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72197-03072197-030-11

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
a9793e44-abad-42de-e053-2a95a90ac940a71dedda-b66e-b710-e053-2995a90ac6602020-07-02WarningsExact identifier
spl id: a9793e44-abad-42de-e053-2a95a90ac940
spl set id: a71dedda-b66e-b710-e053-2995a90ac660

Reported adverse events (FAERS/openFDA)#

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