SPARKLING CRANBERRY HAND SANITIZER- alcohol gel

SPARKLING CRANBERRY HAND SANITIZER by

Drug Labeling and Warnings

SPARKLING CRANBERRY HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Target Corporation, Bath Concept Cosmetics (Dongguan) Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 62%

Purpose

Antiseptic

Uses

• For handwashing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire and flame

do not drink. If taken internally will produce serious gastric disturbance. Does not contain grain alcohol,

When using this product

• Avoid the eyes and mucous membranes
• In the case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop use and ask a doctor if

• Condition worsens
• Redness or irritation develops
• If condition persists for more than 3 days 

Keep out of reach of children

If swallowed contact a doctor or Poison Control Center immediately.

Directions

• Rub dime sized amount between hands until dry.
• Supervise children in the use of this product.
• In the case of eye contact, rinse eyes thoroughly with water.

Other information

• Store below 105 °F
• may discolor some fabrics.

Inactive ingredients

Water, Glycerin, Fragrance, Carbomer, Aminomethyl Propanol, Denatonium Benzoate, Red 40, Red 33.

Questions?

• 1-800-278-9218

Package Labeling:

INGREDIENTS AND APPEARANCE

SPARKLING CRANBERRY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-782
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
FD&C RED NO. 40 (UNII: WZB9127XOA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-782-00	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/28/2020

Labeler - Target Corporation (006961700)

Establishment
Name	Address	ID/FEI	Business Operations
Bath Concept Cosmetics (Dongguan) Co., Ltd		529623933	manufacture(11673-782)