BENZALKONIUM CHLORIDE liquid

Benzalkonium Chloride by

Drug Labeling and Warnings

Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by Family Dollar Stores, Inc, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Claims

FAMILY Wellness™

ANTIBACTERIAL

CITRUS SCENT

LIQUID HAND SOAP REFILL

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• avoid contact with eyes. If contact 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 medical help or contact a Poison Control Center right away.

Directions

• wet hands
• apply palmful to hands
• scrub thoroughly
• rinse thoroughly

Inactive ingredients

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, Citrus nobilis (mandarin orange) oil, Camellia sinensis leaf extract, Zingiber officinale (ginger) root oil, blue 1, yellow 5

Questions?

Call 1-844-636-7687

Adverse Reaction

DISTRIBUTED BY:

MIDWOOD BRANDS, LLC

510 VOLVO PKWY

CHESAPEAKE, VA 23320 USA

MADE IN USA WITH US AND FOREIGN COMPONENTS

100% SATISFACTION OR YOUR MONEY BACK!

NOT 100% SATISFIED?

Return within 30 days to the store of purchase for a refund (with receipt) or exchange.

Disclaimer

*This product is not manufactured or distributed by Colgate-Palmolive Company, distributor of Softsoap ® Antibacterial Fresh Citrus Scent Hand Soap.

Principal Display Panel

FAMILY Wellness™

COMPARE TO SOFTSOAP ® ANTIBACTERIAL FRESH CITRUS SCENT HAND SOAP*

ANTIBACTERIAL

CITRUS SCENT

LIQUID HAND SOAP REFILL

Helps kill harmful germs

Dermatologist tested

With light moisturizers

50 FL OZ (1.56 QT) 1.47 L

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55319-633
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
TETRASODIUM EDTA (UNII: MP1J8420LU)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
DISTEARETH-75 IPDI (UNII: 5365FJ30SC)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BENZOPHENONE-4 (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GINGER OIL (UNII: SAS9Z1SVUK)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CITRUS NOBILIS (MANDARIN ORANGE) OIL (UNII: NJO720F72R)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55319-633-03	1470 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/14/2026

Labeler - Family Dollar Stores, Inc (024472631)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(55319-633)