FDA.reportPublic FDA data

Alcohol

Manufacturer
Rite Aid | Consumer Product Partners, LLC
Effective date
2024-08-07
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 20:57:02

Label at a glance#

ProductAlcohol
Active ingredientALCOHOL
Label structure13 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 thoroghly 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

Questions

OTC - QUESTIONS SECTION

Call 1-866-695-3030

ADVERSE REACTIONS SECTION

DSP-TN-21091  DSP-MO-20087  DSP-MO-28  SDS-MO 20068

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

DISTRIBUTED BY: RITE AID

30 HUNTER LANE

CAMP HILL, PA 17011

www.riteaid.com

look great

feel great

100% GUARANTEE or your money back

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

daylogic

moisturizing

HAND SANITIZER REFILL

WITH VITAMIN E

KILLS 99.99% OF GERMS

Moisturizing Formula with Vitamine E

60FL OZ (1.77 L)

image descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-0015ALCOHOL LIQUID [RITE AID]7Legacy NDC20240809_5ca18b40-210a-4587-b6cb-66da1bc0ad7f.zip

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
11822-001511822-0015-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
TOCOPHEROLR0ZB2556P8IACT
ALCOHOL3K9958V90MACTIB

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
3dfbca5a-e576-f9b3-e063-6294a90ad8325ca18b40-210a-4587-b6cb-66da1bc0ad7f2025-09-04Warnings, Adverse reactionsExact identifier
spl set id: 5ca18b40-210a-4587-b6cb-66da1bc0ad7f

Reported adverse events (FAERS/openFDA)#

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