INODERM CHOICE ANTIBACTERIAL- chloroxylenol liquid

Inoderm Choice Antibacterial by

Drug Labeling and Warnings

Inoderm Choice Antibacterial by is a Otc medication manufactured, distributed, or labeled by Avro Enterprises LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Chloroxylenol 0.3% w/w

Purpose

Antiseptic

Uses

• Handwash to decrease bacteria on the skin that potentially can cause disease.
• Recommended for repeated use.

Warnings

For external use only

When using this product

keep away from eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if 

irritation or redness develop or if 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 with water and dispense small amount of product into cupped palm of hand.
• Lather vigorously for at least 15 seconds.
• Rinse with water and dry thoroughly.

Inactive ingredients

Water, Sodium Lauryl Ether Sulfate, Sodium Chloride, Cocamide MIPA, Sodium Sulfate, Fragrance, Magnesium Nitrate, Citric Acid, FD&C Yellow # 5, Methylchloroisothiazolinone, Magnesium Chloride, Methylsothiazolinone, FD&C Red # 4

Package Labeling:

INGREDIENTS AND APPEARANCE

INODERM CHOICE ANTIBACTERIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73062-523
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
SODIUM SULFATE (UNII: 0YPR65R21J)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73062-523-42	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/14/2023

Labeler - Avro Enterprises LLC (804030166)