FDA.reportPublic FDA data

Rite Aid Isopropyl Alcohol Wipes

Manufacturer
Rite Aid
Effective date
2026-01-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:34:30

Label at a glance#

ProductRite Aid Isopropyl Alcohol Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Indications and uses

first aid to help prevent the risk of infection in: minor cuts scrapes burns

Dosage and administration

clean the affected area apply product on the affected area of the body 1 to 3 times a day may by covered with a sterile bandage if bandaged, let dry frist

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only.

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • do not get in eyes
  • do not apply over large areas
  • do not use longer than 1 week unless directed by a doctor

Stop use and ask doctor if 

OTC - STOP USE SECTION

condition persists or gets worse.

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 product on the affected area of the body 1 to 3 times a day
  • may by covered with a sterile bandage
  • if bandaged, let dry frist

Other information

SPL UNCLASSIFIED SECTION

  • do not apply internally 
  • keep canister tightly closed and stored at room temperature
  • hold away from face when opening

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-844-308-8600

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN4
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD4
797544isopropyl alcohol 70 % Medicated PadSY4
797544isopropyl alcohol 70 % Topical ClothSY4
797544isopropyl alcohol 70 % Topical SwabSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130011822370592GTIN-13: 0011822370592
EAN-13: 0011822370592
GTIN-12: 011822370592
UPC-A: 011822370592
GTIN storage (14 digits): 00011822370592		Label0.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-3709-9Rite Aid Isopropyl Alcohol Wipes4.5 mL in 1 PATCHCLOTH4.54
11822-3709-9Rite Aid Isopropyl Alcohol Wipes40 in 1 CANISTERCLOTH404

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
11822-370911822-3709-9

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
Rite Aid Isopropyl Alcohol WipesISOPROPYL ALCOHOLRite Aidbca837b0-5044-4e97-e053-2a95a90a13af2026-01-22WarningsExact identifier
ndc (package): 11822-3709-9
ndc (product): 11822-3709
ndc11 (package): 11822370909
spl id: 48f8b5d0-370e-c047-e063-6294a90a5170
spl set id: bca837b0-5044-4e97-e053-2a95a90a13af

Reported adverse events (FAERS/openFDA)#

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