Alcohol

Manufacturer
The Kroger Co. | Nice-Pak Products, LLC
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:47:31

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

WARNINGS SECTION

For exterenal use only-hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

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

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

  • do not store above 105⁰F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

ADVERSE REACTION

ADVERSE REACTIONS SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202

QUALITY GUARANTEE

800-362-6900 www.kroger.com

DSP-TN-21091

DSP-MO-20087

DSP-MO-28

SDS-MO-20068

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kroger®

ORIGINAL SCENT

HAND SANITIZER

KILLS 99.99% OF GERMS*

32 FL OZ (946 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN9
247835ethanol 0.62 ML/ML Topical SolutionSCD9
247835ethanol 62 % Topical SolutionSY9
247835ethyl alcohol 62 % Topical SolutionSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-849-16Alcohol59 mL in 1 BOTTLE, PLASTICLIQUID599
30142-849-34Alcohol236 mL in 1 BOTTLE, PUMPLIQUID2369
30142-849-45Alcohol946 mL in 1 BOTTLE, PLASTICLIQUID9469

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30142-84930142-849-16, 30142-849-34, 30142-849-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
AlcoholALCOHOLThe Kroger Co.163b479b-aa0f-4174-8dfb-ac33bd07752a2026-02-27Warnings, Adverse reactionsExact identifier
ndc (package): 30142-849-45
ndc (package): 30142-849-16
ndc (package): 30142-849-34
ndc (product): 30142-849
ndc11 (package): 30142084916
ndc11 (package): 30142084934
ndc11 (package): 30142084945
spl id: 4bd1b42f-47fb-0fc8-e063-6294a90a2eb7
spl set id: 163b479b-aa0f-4174-8dfb-ac33bd07752a

Reported adverse events (FAERS/openFDA)#

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