ANTISEPTIC FOAMING HAND SANITIZER- benzalkonium chloride liquid

Antiseptic Foaming Hand Sanitizer by

Drug Labeling and Warnings

Antiseptic Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Target Corp., Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Claims

• Made without parabens, phthalates, phenoxyethanol or sulfates**
• **Formulated without sulfated surfactants
• Not tested on animals

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin

Warnings

For external use only – hands only

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin

Stop use and ask a doctor if

• skin irritation develops
• If 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
• not recommended for infants

Inactive ingredients

water, glycerin*, diglycerin, disodium cocoamphodiacetate, lauramine oxide, Aloe barbadensis leaf juice*,
sodium benzoate, cetrimonium chloride, citric acid*, methoxy PEG/PPG-7/3 aminopropyl dimethicone, propylene glycol, tetrasodium EDTA, Chamomilla recutita (matricaria) flower extract*, Pyrus malus (apple) fruit extract*, Citrus grandis (grapefruit) peel oil*, Citrus nobilis (mandarin orange) peel oil*, limonene

Claims

*Plant-derived ingredients

†Based on laboratory testing against certain bacteria

ADVERSE REACTIONS

Dist. by Target Corporation

Minneapolis, MN 55403

Made in U.S.A. with U.S. and foreign components.

TM & ©2024

Target Brands, Inc. 

Guest Services

1-800-910-6874

Principal display panel

Alcohol-Free

Foaming Hand Sanitizer

Citrus Scent

• Hypoallergenic
• Made with plant-derived ingredients*
• Kills 99.9% certain germs†
• Dermatologist tested

up&up ™

2-1.5 FL OZ (44 mL) TOTAL 3 FL OZ (88 mL)

INGREDIENTS AND APPEARANCE

ANTISEPTIC FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-812
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIGLYCERIN (UNII: 3YC120743U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE SODIUM (UNII: MP1J8420LU)
CHAMOMILE (UNII: FGL3685T2X)
APPLE (UNII: B423VGH5S9)
CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
MANDARIN OIL (UNII: NJO720F72R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-812-20	2 in 1 CARTON	10/11/2024
1		88 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/11/2024

Labeler - Target Corp. (006961700)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(82442-812)