WALGREENS HAND SANITIZER COASTAL BREEZE SCENT- alcohol gel

Walgreens Hand Sanitizer Coastal Breeze Scent by

Drug Labeling and Warnings

Walgreens Hand Sanitizer Coastal Breeze Scent by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 69% v/v

Purpose

Antiseptic

Uses

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

Warnings

For external use only

Flammable, keep away from fire or flame.

When using this product

• 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

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

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision

Other information

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

Inactive ingredients

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

Company Information

DISTRIBUTED BY: WALGREEN CO.,

200 WILMOT RD., DEERFIELD, IL 60015

Product Packaging

Walgreens

Hand Sanitizer

COASTAL BREEZE

SCENT

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

2 FL OZ (59 ML)

INGREDIENTS AND APPEARANCE

WALGREENS HAND SANITIZER COASTAL BREEZE SCENT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	69 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9006-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/11/2020

Labeler - Walgreen Company (008965063)