FDA.reportPublic FDA data

Kroger 70 Isopropyl Alcohol Wipes

Manufacturer
The Kroger, Co. | Kleen Test Products Corporation
Effective date
2026-01-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:32:36

Label at a glance#

ProductKroger 70 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 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%

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.

Flammablekeep away from fire or flame, heat, spark, electrical

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 of the body
  •  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 be covered with a sterile bandage
  •  if bandaged, let dry first

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

1-800-632-6900

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label01.jpgLabel01.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041260026942GTIN-13: 0041260026942
EAN-13: 0041260026942
GTIN-12: 041260026942
UPC-A: 041260026942
GTIN storage (14 digits): 00041260026942		Label01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-785-00Kroger 70 Isopropyl Alcohol Wipes4.5 g in 1 APPLICATORCLOTH4.51
30142-785-00Kroger 70 Isopropyl Alcohol Wipes40 in 1 CANISTERCLOTH401

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
30142-78530142-785-00

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
WATER059QF0KO0RIACT
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
Kroger 70 Isopropyl Alcohol WipesISOPROPYL ALCOHOLThe Kroger, Co.6ad6fd54-42a4-472a-bb00-95f1224e8f4e2026-01-13WarningsExact identifier
ndc (package): 30142-785-00
ndc (product): 30142-785
ndc11 (package): 30142078500
spl id: 4843791e-fade-8d80-e063-6394a90af8f2
spl set id: 6ad6fd54-42a4-472a-bb00-95f1224e8f4e

Reported adverse events (FAERS/openFDA)#

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