0363-5721-02 Walgreens Hand sanitizer

Manufacturer
Walgreens | Apollo Health and Beauty Care
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:56:41

Label at a glance#

ProductWalgreens
Active ingredientALCOHOL
Label structure8 sections

Storage and handling

do not store above 105F. may discolor some fabric harmful to wood finishes and plastics

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

OTC - PURPOSE SECTION

Antiseptic

WARNINGS SECTION

For External use only : hands

OTC - WHEN USING SECTION

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

OTC - ASK DOCTOR SECTION

if

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed , get medical help or contact a poision Control Centre right away.

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

STORAGE AND HANDLING SECTION

  • do not store above 105F.
  • may discolor some fabric
  • harmful to wood finishes and plastics

INACTIVE INGREDIENT SECTION

Water, PEG-6, AMP-Acrylates/Vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Aloe Barbabensis leaf Powder, Yellow 5, Blue 1

INDICATIONS & USAGE SECTION

  • to reduce bacteria on the skin that could cause disease
  • recommeded for repeated use

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59 ml59 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN6
581662ethanol 0.7 ML/ML Topical GelSCD6
581662ethanol 70 % Topical GelSY6
581662ethyl alcohol 70 % Topical GelSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-5721-02Walgreens59 mL in 1 BOTTLE, PLASTICGEL596

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-57210363-5721-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WalgreensETHYL ALCOHOLwalgreenseb6a653f-b166-db06-e053-2995a90ab87f2026-05-20WarningsExact identifier
ndc (product): 0363-5721
WalgreensETHYL ALCOHOLWalgreenebf222f0-dc46-ee73-e053-2a95a90a07212026-05-08WarningsExact identifier
ndc (product): 0363-5721
WalgreensETHYL ALCOHOLWalgreensebf222f0-dc45-ee73-e053-2a95a90a07212026-05-08WarningsExact identifier
ndc (package): 0363-5721-02
ndc (product): 0363-5721
ndc11 (package): 00363572102
spl id: 51525a09-b43b-2edb-e063-6394a90a4509
spl set id: ebf222f0-dc45-ee73-e053-2a95a90a0721

Reported adverse events (FAERS/openFDA)#

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