ANTIBACTERIAL LHS- benzalkonium chloride liquid

Antibacterial LHS by

Drug Labeling and Warnings

Antibacterial LHS by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION INC., Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Uses

helps eliminate bacteria on hands.

Warnings

For external use only

When using this product

• Avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor if

• irritation or redness develops and lasts.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

• From Liquid Hand Soap pump bottle, apply onto wet hands.
• Lather and rinse thoroughly.

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Hydroxyethylcellulose, Glycerin, Poloxamer 124, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (CI 16035), Red 33 (CI 17200), Yellow 5 (CI 19140).

Questions

1-800-910-6874

Principal Display Panel

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL LHS 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	130 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
POLOXAMER 124 (UNII: 1S66E28KXA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-004-07	222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/01/2024

Labeler - TARGET CORPORATION INC. (006961700)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture(82442-004)