FDA.reportPublic FDA data

Walgreens

Manufacturer
Walgreen Co. | Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:56:20

Label at a glance#

ProductWalgreens Hand Sanitizer Coastal Breeze
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

■ place enough product in your palm ■ rub ihands vigorously until dry ■ children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

For external use only Flammable. Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ place enough product in your palm ■ rub ihands vigorously until dry ■ children under 6 years of age should be supervised when using this product

Other information

SPL UNCLASSIFIED SECTION

■ store below105ºF (40ºC) ■ may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl alcohol, aminomethyl propanol, isopropyl myristate, caprylyl glycol, phenoxyehanol, fragrance, tocopheryl acetate, D&C red no. 33, FD&C blue no. 1

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-1307-022023-01-30C16284748780-1f386c649-c252-0266-e053-dadaa90a7c1aWalgreensDltaCstlBrzeHndsntzr62Alc
0363-1307-082023-01-30C16284748780-1f386c649-c252-0266-e053-dadaa90a7c1aWalgreensDltaCstlBrzeHndsntzr62Alc
0363-1307-282023-01-30C16284748780-1f386c649-c252-0266-e053-dadaa90a7c1aWalgreensDltaCstlBrzeHndsntzr62Alc

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-1307WALGREENS HAND SANITIZER COASTAL BREEZE (ALCOHOL) LIQUID [WALGREEN CO.]2Legacy NDC20210116_b25c4b9f-9fa8-57b4-e053-2a95a90a80ce.zip

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
0363-13070363-1307-02, 0363-1307-08, 0363-1307-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
CAPRYLYL GLYCOL00YIU5438UIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
b8f3de8f-3d62-2855-e053-2a95a90a3f1db25c4b9f-9fa8-57b4-e053-2a95a90a80ce2021-01-15WarningsExact identifier
spl id: b8f3de8f-3d62-2855-e053-2a95a90a3f1d
spl set id: b25c4b9f-9fa8-57b4-e053-2a95a90a80ce

Reported adverse events (FAERS/openFDA)#

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