50% Rubbing Alcohol First Aid Antiseptic

Manufacturer
Pride Products Corp.
Effective date
2024-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:13

Label at a glance#

Product50% Rubbing Alcohol First Aid Antiseptic
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol (50% conc.)

OTC - PURPOSE SECTION

First aid antiseptic

INDICATIONS & USAGE SECTION

USES

  • first aid to help prevent the risk of infection in minor cuts, scrapes, and burns
  • helps relieve minor muscular aches due to exertion

WARNINGS SECTION

Warnings

For external use only.

Flammable, keep away from heat, spark, electrical, fire or flame.

  • helps relieve minor muscular aches due to exertion.

OTC - DO NOT USE SECTION

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week
  • do not inhale

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • the condition persists or gets worse
  • irritation, pain, or redness persists or worsens
  • swelling, rash, or fever develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • clean the affected area
  • apply a small amount of product on the affected area 1 to 3 times a day
  • may be covered with a sterile bandage
  • if bandaged, let dry first

OTHER SAFETY INFORMATION

Other information

  • keep tightly closed at controlled room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

INACTIVE INGREDIENT SECTION

Purified water, methyl salicylate, FD&C Blue #1, FD&C Yellow #5.

RECENT MAJOR CHANGES SECTION

Incorrect heading selected

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50%50%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50% ISOPROPYL RUBBING ALCOHOL

First Aid Antiseptic

For Rubbing & Massaging

WINTERGREEN

Use only in a well ventilated area; fumes may be harmful.

CAUTION: Do not point at self or others; product will squirt when squeezed.

WARNING: FLAMMABLE

KEEP AWAY FROM HEAT, SPARK, ELECTRICAL, FIRE OR FLAME

12 FL OZ (355 mL)

Alcohol's effectiveness at killing germs *drops sharply when diluted below 50% concentration, *and the optimal concentration for killing bacteria is between 60 to 90 percent, according to CDC. For hand sanitization purposes, a 70% dilution is recommended. *This product is intended for massaging, minor cuts and other cleaning purposes.

Manufactured for:

NEW PRIDE CORP.

RONKONKOMA, NY 11779

prideproducts.com

A PROUD AMERICAN COMPANY

Made in Jordan

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58037-702-012025-07-29C16284748780-13b156c62-2b3d-fb37-e063-e6dba90a4e07Pride Products Corp. 50% Isopropyl Rubbing Alcohol First Aid Antiseptic (Wintergreen)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58037-702-0150% Rubbing Alcohol First Aid Antiseptic355 mL in 1 BOTTLELIQUID3552

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58037-70250% RUBBING ALCOHOL FIRST AID ANTISEPTIC (ISOPROPYL ALCOHOL) LIQUID [PRIDE PRODUCTS CORP.]21 package rows20240115_0e7c5f52-8982-0e0a-e063-6294a90a5797.zip

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
58037-70258037-702-01

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
0e7d2f0d-278d-536e-e063-6294a90ac0ee0e7c5f52-8982-0e0a-e063-6294a90a57972024-01-08WarningsExact identifier
spl id: 0e7d2f0d-278d-536e-e063-6294a90ac0ee
spl set id: 0e7c5f52-8982-0e0a-e063-6294a90a5797

Reported adverse events (FAERS/openFDA)#

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