GLOBAL CARE GOLD ANTIBACTERIAL HAND- benzalkonium chloride liquid

GLOBAL CARE GOLD ANTIBACTERIAL HAND by

Drug Labeling and Warnings

GLOBAL CARE GOLD ANTIBACTERIAL HAND by is a Otc medication manufactured, distributed, or labeled by TARGET PRICE, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts 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 eye contact, flush with water.

Stop use and ask a doctor if

irritation and redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands as needed
• lather vigorously for at least 15 seconds
• rinse and dry thoroughly.

Inactive ingredients

Water (Aqua), Cocamidopropyl Betaine, Sodium Cocoamphoacetate, PEG-150 Distearate, Fragrance, PEG-40 Hydrogenated Castor Oil, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No. 5, FD&C Red No.40

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLOBAL CARE GOLD ANTIBACTERIAL HAND 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72146-100
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
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
WATER (UNII: 059QF0KO0R)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72146-100-01	400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/01/2024

Labeler - TARGET PRICE, INC. (081086884)

Registrant - TARGET PRICE, INC. (081086884)