Inoderm Choice Antibacterial

Manufacturer
Avro Enterprises LLC
Effective date
2023-10-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:58:13

Label at a glance#

ProductInoderm Choice Antibacterial
Active ingredientCHLOROXYLENOL
Label structure6 sections

Indications and uses

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

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if 

OTC - STOP USE SECTION

irritation or redness develop or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

INACTIVE INGREDIENT SECTION

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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
413261chloroxylenol 0.3 % Medicated Liquid SoapPSN2
413261chloroxylenol 3 MG/ML Medicated Liquid SoapSCD2
413261chloroxylenol 0.3 % Medicated Liquid SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73062-523-42Inoderm Choice Antibacterial3800 mL in 1 BOTTLELIQUID38002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73062-523INODERM CHOICE ANTIBACTERIAL (CHLOROXYLENOL) LIQUID [AVRO ENTERPRISES LLC]2Current NDC, 1 package rows20231030_829056d2-3d01-47e1-a23d-ea06c3896355.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73062-52373062-523-42

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Inoderm Choice AntibacterialCHLOROXYLENOLAvro Enterprises LLC829056d2-3d01-47e1-a23d-ea06c38963552023-10-28WarningsExact identifier
ndc (package): 73062-523-42
ndc (product): 73062-523
ndc11 (package): 73062052342
spl id: 08bff442-7d38-56d5-e063-6394a90a6477
spl set id: 829056d2-3d01-47e1-a23d-ea06c3896355

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.