FDA.reportPublic FDA data

RUBBING ALCOHOL

Manufacturer
Viny Health and Beauty Products Inc
Effective date
2017-11-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:09:51

Label at a glance#

ProductRUBBING ALCOHOL 99 PERCENT
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

FIRST AID TO HELP PREVENT THE RISK IN: MINOR CUTS SCRAPES BURNS

Dosage and administration

CLEAN AFFECTED AREA APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 TIMES DAILY MAY BE COVERED WITH A STERILE BANDAGE IF BANDAGED, LET DRY FIRST

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ISOPROPYL ALCOHOL 99%

Purpose

OTC - PURPOSE SECTION

FIRST AID ANTISEPTIC

Uses

INDICATIONS & USAGE SECTION

FIRST AID TO HELP PREVENT THE RISK IN:

  • MINOR CUTS
  • SCRAPES
  • BURNS

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.

WARNINGS

WARNINGS SECTION

For external use only.

FLAMMABLE

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

FOR RUBBING AND MASSAGING: CAUTION - DO NOT APPLY TO IRRITATED SKIN OR IF EXCESSIVE IRRITATION DEVELOPS. AVOID GETTING INTO THE EYES OR ON MUCOUS MEMBRANES.

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

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 GET WORSE.

Directions

DOSAGE & ADMINISTRATION SECTION

  • CLEAN AFFECTED AREA
  • APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 TIMES DAILY
  • MAY BE COVERED WITH A STERILE BANDAGE
  • IF BANDAGED, LET DRY FIRST

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • DOES NOT CONTAIN, NOR IS INTENDED AS A SUBSTITUTE FOR GRAIN OR ETHYL ALCOHOL
  • WILL PRODUCE SERIOUS GASTRIC DISTURBANCES IF TAKEN INTERNALLY.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

PURIFIED WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IPA Regular 99pct_16ozIPA Regular 99pct_16oz

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
76436-30676436-306-16

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
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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
2be86c99-3b14-4cca-97eb-9463835b362dacc8a538-0f3c-4acc-bc23-8b8cd13eeacb2021-01-10WarningsExact identifier
spl set id: acc8a538-0f3c-4acc-bc23-8b8cd13eeacb

Reported adverse events (FAERS/openFDA)#

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