BYD Antibacterial Wet Wipes

Manufacturer
Shanwei BYD Industrial Co Ltd.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:17:42

Label at a glance#

ProductBYD Antibacterial Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and uses

For hand washing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry. For children under 6, use only under adult supervision.

Storage and handling

For dispensing, peel back front at tab. Remove wipes as needed. Reseal pouch by pressing label firmly back into place.

Label contents#

Full prescribing information#

Misc.

SPL UNCLASSIFIED SECTION

Manufactured by:

Shanwei BYD Industrial Co., Ltd.

516626, Hongcao Industrial Park, No. 22 Sanhe Road, Shanwei High-Tech Development Zone, Shanwei City, China

Tel: +86-755-89888888

Website: www.byd.com

Made in China

Distributed by Global Healthcare Product Solutions, LLC

1 (800) 293-2886

01_101_101_201_2

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% (w/w)

0202

Purpose:

OTC - PURPOSE SECTION

Antiseptic

0303

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

0404

Warnings:

WARNINGS SECTION

For external use only

0505

When using this product:

OTC - DO NOT USE SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

0606

When using this product:

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

0707

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Irritation or redness develops.

0808

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.

0909

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.

For children under 6, use only under adult supervision.

1010

Other information:

STORAGE AND HANDLING SECTION

For dispensing, peel back front at tab. Remove wipes as needed. Reseal pouch by pressing label firmly back into place.

1111

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Decyl glucoside, glycerin, methylparaben, propylparaben, phenoxyethanol, tocopheryl acetate, water.

1212

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

13_113_113_213_213_313_313_413_413_513_5

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
73818-30573818-305-01
73818-30673818-306-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
ffaeb449-790f-090b-e053-6294a90a5e78b8fa31df-ae4b-5436-e053-2995a90ab9172023-07-04WarningsExact identifier
spl set id: b8fa31df-ae4b-5436-e053-2995a90ab917

Reported adverse events (FAERS/openFDA)#

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