HAND RX ANTIBACTERIAL SKIN- benzalkonium chloride lotion

HAND RX ANTIBACTERIAL SKIN by

Drug Labeling and Warnings

HAND RX ANTIBACTERIAL SKIN by is a Otc medication manufactured, distributed, or labeled by PRIMAL ELEMENTS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only - hands.

Flammable. Keep away from heat and flame.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

skin irritation develops.

Keep out of reach of children.

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

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not store above 105℉
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

Water(Aqua), Mineral Oil, Cetearyl Alcohol, Petrolatum, Glyceryl Stearate, Ceteareth-25, Ammonium Polyacrylate, C13-16 Isoparaffin, Laureth-30, Fragrance, Glycerin, Carbomer, Propylene Glycol, Dimethicone, Methylisothiazolinone, Iodopropynyl Butylcarbamate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND RX ANTIBACTERIAL SKIN 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80801-106
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 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHICONE (UNII: 92RU3N3Y1O)
C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
LAURETH-30 (UNII: W9D845551A)
CARBOMER 940 (UNII: 4Q93RCW27E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PETROLATUM (UNII: 4T6H12BN9U)
CETEARETH-25 (UNII: 8FA93U5T67)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80801-106-01	118 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/20/2024

Labeler - PRIMAL ELEMENTS (968334144)