CVS Health Isopropyl Rubbing Alcohol - CVS Pharmacy, Inc

Manufacturer
CVS Pharmacy, Inc
Effective date
2026-09-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-25 02:01:06

Label at a glance#

ProductCVS Health Isopropyl Rubbing Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70% by volume

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable,keep away from heat, spark, electrical, fire or flame 

  • will produce serious gastric disturbances if taken internally

Do not use

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Nitrogen, Purified Water, Sodium Benzoate

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428440346GTIN-13: 0050428440346
EAN-13: 0050428440346
GTIN-12: 050428440346
UPC-A: 050428440346
GTIN storage (14 digits): 00050428440346
Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-97951316-979-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-03-22full-release2026-06-01 00:10:55

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
14421293-d206-eee5-e063-6294a90a76f12bd271ff-bb2e-426b-a7ad-87bb7dfb3df62024-03-22WarningsExact identifier
spl set id: 2bd271ff-bb2e-426b-a7ad-87bb7dfb3df6

Reported adverse events (FAERS/openFDA)#

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