INODERM STYLE ANTIBACTERIAL- chloroxylenol liquid 
Inopak, Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Inopak Style Antibacterial Liquid Soap

Drug Facts

Active ingredient

Chloroxylenol 0.3% w/w

Purpose

Antiseptic

Uses

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

Inactive ingredients

Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamide DEA, DMDM Hydantoin, Alcohol, Fragrance, Isopropyl Alcohol, Citric Acid, FD&C Yellow 5, FD&C Red 4.

Inopak, LTD.

Ringwood, NJ 07456

1-800-762-7725 • www.inopak.com

INODERM®

With Moisturizers

Style

Contains Chloroxylenol 0.3%

Liquid Antibacterial Soap

18 fl. oz. (532 mL)

InoDerm Style Soap 18oz 2021

INODERM STYLE ANTIBACTERIAL 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58575-523
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCO DIETHANOLAMIDE (UNII: 92005F972D)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
ALCOHOL (UNII: 3K9958V90M)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58575-523-423800 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/202107/22/2024
2NDC:58575-523-07237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/202110/08/2023
3NDC:58575-523-17532 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/202107/19/2024
4NDC:58575-523-801 in 1 BOX04/20/202101/28/2024
4800 mL in 1 POUCH; Type 0: Not a Combination Product
5NDC:58575-523-822000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/20/202104/21/2024
6NDC:58575-523-101000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/20/202111/06/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/20/202107/22/2024
Labeler - Inopak, Ltd (194718243)
Establishment
NameAddressID/FEIBusiness Operations
Inopak, Ltd194718243manufacture(58575-523)

Revised: 2/2023
Document Id: f5178976-cb3c-2b26-e053-2995a90aba5f
Set id: c05c2548-aada-691f-e053-2995a90a1c58
Version: 2
Effective Time: 20230219
 
Inopak, Ltd