Purdoux

Manufacturer
Choice One Medical Inc | ZHEJIANG RUOLIN HYGIENIC PRODUCTS CO., LTD
Effective date
2023-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:40:33

Label at a glance#

ProductPurdoux
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Flip open dispensing cap. Locate wipe at center of roll via small opening of the lid. Close the lid cap after use. Apply to hands and skin. No rinsing required. Discard after use. Children under 6 years of age should be supervised when using this product.

Storage and handling

Avoid freezing and store below 110 F (43 Celcius). Dispose of the used wipe in the trash, do not flush it into the toilet.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

on children less than two months of age
near eyes or on on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 800-222-1222

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Flip open dispensing cap. Locate wipe at center of roll via small opening of the lid. Close the lid cap after use.
Apply to hands and skin. No rinsing required. Discard after use.

Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Avoid freezing and store below 110 F (43 Celcius).

Dispose of the used wipe in the trash, do not flush it into the toilet.

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe babadensis leaf juice, ethylhexylglycerin, fragrance, glycerin, propylene glycol, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 PCS NDC: 81796-111-1180 PCS NDC: 81796-111-1180 PCS NDC: 81796-124-13

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81796-12481796-124-11, 81796-124-12, 81796-124-13, 81796-124-14, 81796-124-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
f228641e-ebf7-3f4a-e053-2995a90a251ff228641e-ebf8-3f4a-e053-2995a90a251f2023-01-13WarningsExact identifier
spl id: f228641e-ebf7-3f4a-e053-2995a90a251f
spl set id: f228641e-ebf8-3f4a-e053-2995a90a251f

Reported adverse events (FAERS/openFDA)#

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