INODERM STYLE ANTIBACTERIAL- chloroxylenol liquid

Inoderm Style Antibacterial by

Drug Labeling and Warnings

Inoderm Style 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

For handwashing to help reduce bacteria on the skin. 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, Methylisothiazolinone, FD&C Red # 4

Package Labeling:

INGREDIENTS AND APPEARANCE

INODERM STYLE ANTIBACTERIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73062-055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 mg  in 0.001 L

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: 73062-055-00	3.8 L in 1 BOTTLE; Type 0: Not a Combination Product	03/16/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/16/2023

Labeler - Avro Enterprises LLC (804030166)