Rubbing Alcohol

Manufacturer
Nobum Labs, S.A.P.I. de C.V.
Effective date
2022-01-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:42

Label at a glance#

ProductRubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Dosage and administration

* clean affected area *apply small amount of this product on the area 1-3 times daily * If bandaged, lets dry first may be covered with a sterile bandage

Storage and handling

store at room temperature does not contain, nor is intended as a sustitute for grain or ethyl alcohol.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v. Purpose: First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only.

Keep away from heat or flame. If taken internally serious gastric disturbances will result.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

OTC - WHEN USING SECTION

* 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

In case of ingestion, get medical help or call Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

* clean affected area

*apply small amount of this product on the area 1-3 times daily

* If bandaged, lets dry first may be covered with a sterile bandage

Other information

STORAGE AND HANDLING SECTION

store at room temperature does not contain, nor is intended as a sustitute for grain or ethyl alcohol.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water.

Package Label - Principal Display Panel 500 ml NDC: 81213-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 ml NDC: 81213-001-01

Rubbing_AlcoholRubbing_Alcohol

946 mL NDC: 81213-001-02

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

946 mL NDC: 81213-001-02

Rubbing_AlcoholRubbing_Alcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN2
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD2
808520isopropyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81213-001-012023-07-28C16284748780-10191ceaa-6323-198a-e063-dbdaa90aec3eRubbing Alcohol (IPA )
81213-001-022023-07-28C16284748780-10191ceaa-6323-198a-e063-dbdaa90aec3eRubbing Alcohol (IPA )

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81213-001-01Rubbing Alcohol500 mL in 1 BOTTLELIQUID5002
81213-001-02Rubbing Alcohol946 mL in 1 BOTTLELIQUID9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81213-001RUBBING ALCOHOL (ISOPROPYL ALCOHOL) LIQUID [NOBUM LABS, S.A.P.I. DE C.V.]2Legacy NDC, 2 package rows20220128_b555ef03-ceb5-77d9-e053-2995a90a13d5.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
81213-00181213-001-01, 81213-001-02

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
d69523ea-ef7f-f06f-e053-2a95a90ac931b555ef03-ceb5-77d9-e053-2995a90a13d52022-01-27WarningsExact identifier
spl id: d69523ea-ef7f-f06f-e053-2a95a90ac931
spl set id: b555ef03-ceb5-77d9-e053-2995a90a13d5

Reported adverse events (FAERS/openFDA)#

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