INODERM Style Antibacterial
- Manufacturer
- Inopak, Ltd
- Effective date
- 2023-02-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:36:17
Label at a glance#
ProductINODERM Style Antibacterial
Active ingredientCHLOROXYLENOL
Label structure9 sections
Contacts and useful links#
Websitewww.inopak.com
www.inopak.com
www.inopak.comLabel contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Chloroxylenol 0.3% w/w
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
- For handwashing to help reduce bacteria on the skin.
- Recommended for repeat use.
WARNINGS SECTION
Warnings
For external use only.
OTC - WHEN USING SECTION
When using this product, keep away from eyes. In case of eye contact, flush eyes with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develop or if condition persists for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
- Wet hands with water and dispense sufficient amount of product into cupped palm of hand.
- Lather vigorously for at least 15 seconds.
- Rinse with water and dry thoroughly.
INACTIVE INGREDIENT SECTION
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.
SPL UNCLASSIFIED SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INODERM®
With Moisturizers
Style
Contains Chloroxylenol 0.3%
Liquid Antibacterial Soap
18 fl. oz. (532 mL)
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- INODERM Style Antibacterial
- Chloroxylenol
- CITRIC ACID MONOHYDRATE
- COCO DIETHANOLAMIDE
- DMDM HYDANTOIN
- ALCOHOL
- FD&C RED NO. 4
- FD&C YELLOW NO. 5
- ISOPROPYL ALCOHOL
- SODIUM CHLORIDE
- SODIUM LAURETH SULFATE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 58575-523 | 58575-523-42, 58575-523-07, 58575-523-17, 58575-523-80, 58575-523-82, 58575-523-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| COCO DIETHANOLAMIDE | 92005F972D | IACT |
| DMDM HYDANTOIN | BYR0546TOW | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| FD&C RED NO. 4 | X3W0AM1JLX | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM LAURETH SULFATE | BPV390UAP0 | IACT |
| WATER | 059QF0KO0R | IACT |
| CHLOROXYLENOL | 0F32U78V2Q | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| f5178976-cb3c-2b26-e053-2995a90aba5f | c05c2548-aada-691f-e053-2995a90a1c58 | 2023-02-19 | Warnings | f5178976-cb3c-2b26-e053-2995a90aba5f c05c2548-aada-691f-e053-2995a90a1c58 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.