Handi-Kleen Antibacterial
- Manufacturer
- Diamond Chemical Co. Inc.
- Effective date
- 2022-09-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:53:03
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Cloroxylenol 0.3% w/w
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
- Handwash to help reduce bacteria on the skin that potentially can cause disease.
- Recommended for repeated use.
WARNINGS SECTION
Warnings
For external use only.
OTC - WHEN USING SECTION
When using this product keep out of 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.
- Wash both hands thoroughly for 15 minutes.
- Rinse under running water and dry thoroughly.
INACTIVE INGREDIENT SECTION
Inactive Ingredients Water, Sodium Laureth Sulfate, Cocamide DEA, DMDM Hydantoin, Ethyl Alcohol, Phenoxyethanol, Isopropyl Alcohol, Fragrance, Citric Acid, FD&C Red 4
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Handi-Kleen™
Antibacterial Foaming Hand Wash
1000 ML (33.8 FL.OZ.) CARTRIDGE
DISTRIBUTED BY:
STARCO CHEMICAL
A Division of Diamond Chemical Co., Inc.
Union Ave & Dubois Street East Rutherford, NJ 07073 • (201) 935-4300
Products#
Every source-derived product name is available through these pages.
- Handi-Kleen Antibacterial Foaming Hand Wash
- Chloroxylenol
- CITRIC ACID MONOHYDRATE
- COCAMIDOPROPYL DIMETHYLAMINE
- DMDM HYDANTOIN
- ALCOHOL
- ISOPROPYL ALCOHOL
- PHENOXYETHANOL
- FD&C RED NO. 4
- SODIUM LAURETH SULFATE
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72177-180 | 72177-180-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| COCAMIDOPROPYL DIMETHYLAMINE | L36BM7DG2T | IACT |
| DMDM HYDANTOIN | BYR0546TOW | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| FD&C RED NO. 4 | X3W0AM1JLX | 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 |
|---|---|---|---|---|---|---|
| e99b21f7-5d92-95da-e053-2995a90a944a | ba6fcc25-4a32-57f6-e053-2995a90ae913 | 2022-09-26 | Warnings | e99b21f7-5d92-95da-e053-2995a90a944a ba6fcc25-4a32-57f6-e053-2995a90ae913 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
