UP AND UP- benzalkonium chloride liquid

UP and UP by

Drug Labeling and Warnings

UP and UP 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

• For hand washing to decrease bacteria on the skin.

Warnings

For external use only

When using this product

• Avoid contact with eyes. In case of contact, flush with water.

Stop use and ask a doctor

if irritation or redness develops and lasts 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

• Apply onto dry hands.
• Lather and rinse thoroughly with water.

Inactive Ingredients.

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

Questions

1-800-910-6874

Principal Display Panel

INGREDIENTS AND APPEARANCE

UP AND UP 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-088
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
WATER (UNII: 059QF0KO0R)
HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
RED 40 (UNII: WZB9127XOA)
RED 33 (UNII: 9DBA0SBB0L)
POLOXAMER 124 (UNII: 1S66E28KXA)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
TETRASODIUM EDTA (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID (UNII: 2968PHW8QP)
YELLOW 5 (UNII: I753WB2F1M)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-088-07	222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/22/2025

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(82442-088)