FDA.reportPublic FDA data

RUBBING ALCOHOL

Manufacturer
SAGE OIL LLC
Effective date
2015-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:32:26

Label at a glance#

ProductRUBBING ALCOHOL 50 PERCENT
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

FIRST AID TO HELP THE RISK OF INFECTION IN MINOR CUTS AND SCRAPES.

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 (BY VOLUME)

OTC - ACTIVE INGREDIENT SECTION

ISOPROPYL ALCOHOL (50% CONCENTRATE)

Purpose

OTC - PURPOSE SECTION

FIRST AID ANTISEPTIC

Uses

INDICATIONS & USAGE SECTION

FIRST AID TO HELP THE RISK OF INFECTION IN MINOR CUTS AND SCRAPES.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

IN CASE OF INGESTION, GET MEDICAL HELP OR CONTACT A POSON CONTROL CENTER (1-800-222-1222) IMMEDIATELY.

WARNINGS

WARNINGS SECTION

For external use only.

  • FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME
  • IF TAKEN NTERNALLY 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

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

  • STORE AT ROOM TEMPERATURE
  • DOES NOT CONTAIN, NOR IS INTENDED AS A SUBSTITUTE FOR GRAIN OR ETHYL ALCOHOL

Inactive Ingredient

INACTIVE INGREDIENT SECTION

PURIFIED WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Medi Bond 50pct Rubbing Alcohol_LabelMedi Bond 50pct Rubbing Alcohol_Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69730-301-122024-11-29C16284748780-19d75b9d0-f8a4-f424-e053-dadaa90a57ce7f59fba6-0bea-442d-b156-92ee503ad8ef
69730-301-122020-01-31C16284748780-19d75b9d0-f8a4-f424-e053-dadaa90a57ce7f59fba6-0bea-442d-b156-92ee503ad8ef

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
WATERINACTIVE INGREDIENT059QF0KO0R1

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
69730-30169730-301-12

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
2816b7ab-1420-a3c2-e063-6394a90aa1f37f59fba6-0bea-442d-b156-92ee503ad8ef2024-11-29WarningsExact identifier
spl set id: 7f59fba6-0bea-442d-b156-92ee503ad8ef

Reported adverse events (FAERS/openFDA)#

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