ANTIBACTERIAL BERRY MEDLEY- benzalkonium chloride liquid

ANTIBACTERIAL BERRY MEDLEY by

Drug Labeling and Warnings

ANTIBACTERIAL BERRY MEDLEY by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warning

For external use only

When using this product  avoid contact with eyes in case of eye contact, flush with water

Stop use and ask a doctor if  irritation or redness develops 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 and apply soap  lather all surfaces of hands and fingers by rubbing vigorously for at least 20 seconds  rinse hands well and dry

Inactive ingredients

Water(Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide Methyl MEA, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, Fragrance, Sodium Chloride, D&C Red No.33, FD&C Blue No. 1.

SPL UNCLASSIFIED SECTION

NEW

kill Germs and Odors

Distributed by:
Universal Distribution Center LLC
330 Applegarth Road, Monroe Township, NJ08831

www.universaldc.com

Made in China

Packaging

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL BERRY MEDLEY 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-436
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-436-64	1893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/31/2026

Labeler - Universal Distribution Center LLC (019180459)