FDA.reportPublic FDA data

Walgreens Hand Sanitizer Coastal Breeze Scent

Manufacturer
Walgreen Company
Effective date
2020-08-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:30

Label at a glance#

ProductWalgreens Hand Sanitizer Coastal Breeze Scent
Active ingredientALCOHOL
Label structure9 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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 69% v/v

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 external use only

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

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Denatonium Benzoate, Blue 1, Yellow 5.

Company Information

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: WALGREEN CO.,

200 WILMOT RD., DEERFIELD, IL 60015

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

Hand Sanitizer

COASTAL BREEZE

SCENT

  • Leaves hands soft
  • Contains moisturizers
  • Kills 99.9% of common germs

2 FL OZ (59 ML)

sanitizer coastal breezesanitizer coastal breeze

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2287763ethanol 69 % Topical GelPSN1
2287763ethanol 0.69 ML/ML Topical GelSCD1
2287763ethanol 69 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-9006-012022-01-28C16284748780-1d6a99b39-7995-a426-e053-dadaa90af4c2Walgreens Hand Sanitizer Coastal Breeze Scent

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9006-01Walgreens Hand Sanitizer Coastal Breeze Scent59 mL in 1 BOTTLE, PLASTICGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-9006WALGREENS HAND SANITIZER COASTAL BREEZE SCENT (ALCOHOL) GEL [WALGREEN COMPANY]1Legacy NDC, 1 package rows20200812_ac9dfce5-d07c-46d3-e053-2a95a90a06f9.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-90060363-9006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
ac9e0ce0-d24c-238f-e053-2995a90acaabac9dfce5-d07c-46d3-e053-2a95a90a06f92020-08-11WarningsExact identifier
spl id: ac9e0ce0-d24c-238f-e053-2995a90acaab
spl set id: ac9dfce5-d07c-46d3-e053-2a95a90a06f9

Reported adverse events (FAERS/openFDA)#

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