FDA.reportPublic FDA data

BYD Antibacterial Wet Wipes

Manufacturer
Shanwei BYD Industrial Co Ltd
Effective date
2020-09-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:14:53

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

After unseal, tighten the cap and use product within the validity period.

Label contents#

Full prescribing information#

Misc.

SPL UNCLASSIFIED SECTION

Expiration Date

2 years after date of production

Distributed by Global Healthcare Product Solutions, LLC

1 (800) 293-2886

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

0101

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% (w/w)

02_102_1

Purpose:

OTC - PURPOSE SECTION

Antibacterial

02_202_2

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

02_302_3

Warnings:

WARNINGS SECTION

For external use only

02_402_4

When using this product:

OTC - DO NOT USE SECTION

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

02_502_5

When using this product:

OTC - WHEN USING SECTION

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

02_602_6

Stop use and ask a doctor if:

OTC - STOP USE SECTION

Irritation or redness develops.

02_702_7

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help right away.

02_802_8

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.

For children under 6, use only under adult supervision.

02_902_9

Other information:

STORAGE AND HANDLING SECTION

After unseal, tighten the cap and use product within the validity period.

02_1002_10

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Glycerin, water.

02_1102_11

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

030304040505

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73818-303-012023-07-05C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-303-022023-07-05C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-304-012023-07-05C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-304-022023-07-05C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-303-012022-01-28C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-303-022022-01-28C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-304-012022-01-28C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e
73818-304-022022-01-28C16284748780-1d6a99b39-7c1d-a426-e053-dadaa90af4c2afc80b8b-da38-6fb9-e053-2a95a90a2d8e

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73818-30373818-303-01, 73818-303-02
73818-30473818-304-01, 73818-304-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ffc207a4-9815-d8ee-e053-6294a90ab131afc80b8b-da38-6fb9-e053-2a95a90a2d8e2023-07-05WarningsExact identifier
spl set id: afc80b8b-da38-6fb9-e053-2a95a90a2d8e

Reported adverse events (FAERS/openFDA)#

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