FDA.reportPublic FDA data

99 PERCENT ISOPROPYL RUBBING ALCOHOL

Manufacturer
Viny Health and Beauty Products Inc
Effective date
2023-12-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:17:15

Label at a glance#

Product99 PERCENT ISOPROPYL RUBBING ALCOHOL with Wintergreen Oil
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

CLEAN THE AFFECTED AREA APPLY A SMALL AMOUNT OF THIS PRODUCT TO THE AREA 1 TO 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

WARNINGS

WARNINGS SECTION

For external use only.

FLAMMABLE

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

ASK A DOCTOR BEFORE USE IF YOU HAVE DEEP OR PUNCTURE WOUNDS, ANIMAL BITES OR SERIOUS BURNS.

WHEN USING THIS PRODUCT

  • DO NOT GET INTO EYES
  • DO NOT APPLY OVER LARGE AREAS OF THE BODY
  • DO NOT USE LONGER THAN 1 WEEK UNLESS DIRECTED BY A DOCTOR

STOP USE AND ASK A DOCTOR IF CONDITION PERSISTS OR GETS WORSE.

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

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • CLEAN THE AFFECTED AREA
  • APPLY A SMALL AMOUNT OF THIS PRODUCT TO THE AREA 1 TO 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

BLUE 1, METHYL SALICYLATE, WATER, YELLOW 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Sofskin_99 percent_Wintergreen_16oz01b LBL_Sofskin_99 percent_Wintergreen_16oz

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
76436-31276436-312-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
METHYL SALICYLATELAV5U5022YIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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
1279bc2d-c9aa-73c9-e063-6394a90ae54ade0cf28c-4134-0c93-e053-2a95a90a0e7f2024-02-28WarningsExact identifier
spl set id: de0cf28c-4134-0c93-e053-2a95a90a0e7f

Reported adverse events (FAERS/openFDA)#

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