Puresan Antibacterial Liquid
- Manufacturer
- Avro Enterprises LLC
- Effective date
- 2023-01-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:39:50
Label at a glance#
ProductPuresan Antibacterial Liquid
Active ingredientCHLOROXYLENOL
Label structure9 sections
Contacts and useful links#
Label 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 repeated 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
Distributed By: Puresan
24 Ames Blvd., Hamburg, NJ 07419
855.500.8080 • puresanusa.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Antibacterial Liquid Soap
With Moisturizers
Contains Chloroxylenol 0.3%
33.8 fl.oz. (1000 mL) Refill Bag LIQUID
Products#
Every source-derived product name is available through these pages.
- Puresan Antibacterial Liquid
- Chloroxylenol
- CITRIC ACID ACETATE
- 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 |
|---|---|
| 73062-408 | 73062-408-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID ACETATE | DSO12WL7AU | 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 |
|---|---|---|---|---|---|---|
| f27977ed-9611-3c5b-e053-2995a90a419d | ca039354-6456-5a42-e053-2995a90a8106 | 2023-01-02 | Warnings | f27977ed-9611-3c5b-e053-2995a90a419d ca039354-6456-5a42-e053-2995a90a8106 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.