SIMPLIFY WHITE TEA LHS- benzalkonium chloride liquid

Simplify White Tea LHS by

Drug Labeling and Warnings

Simplify White Tea LHS by is a Otc medication manufactured, distributed, or labeled by RITE AID CORPORATION, Apollo Health and Beauty Care. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

For Handwashing to decrease bacteria on the skin.

Warnings

For externaluse only: hands only.

When using the product

• Avoid contact with eyes. If this occurs, rinse eyes with water.

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 mdical help or contact a Poison Control Center right away.

Directions

• Wet Hands,
• Apply palmful to hands.
• Scrub thoroughly.
• rinse thoroughly.

Inactive Ingredients

Blue 1 (CI 42090), Citric Acid, Cocamidopropyl Betaine, Fragrance, Glycerin, Hydroxyethylcellulose, Methylchloroisothiazolinone, Methylisothiazolinone, Poloxamer 124, Red 33 (CI 17200), Tetrasodium EDTA, Water.

Questions or comments?

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INGREDIENTS AND APPEARANCE

SIMPLIFY WHITE TEA LHS 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-2000
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
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
BLUE 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
TETRASODIUM EDTA (UNII: MP1J8420LU)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID (UNII: 2968PHW8QP)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLOXAMER 124 (UNII: 1S66E28KXA)
RED 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-2000-1	332 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/16/2025

Labeler - RITE AID CORPORATION (014578892)

Registrant - Apollo Health and Beauty Care (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
Apollo Health and Beauty Care		201901209	manufacture(11822-2000)