FDA.reportPublic FDA data

BYD Antibacterial Wet Wipes (Children)

Manufacturer
BYD Automative Industry Co., Ltd.
Effective date
2020-09-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:49

Label at a glance#

ProductBYD Antibacterial Wet Wipes (Children)
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

Manufactured by:

BYD Auto Industry Company Limited

No. 3001, 3007, Hengping Road,

Pingshan, Shenzhen, 518118, P.R. 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

Antibacterial

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 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

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

1111

Inactive ingredients:

INACTIVE INGREDIENT SECTION

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

1212

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

13_113_113_213_2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75035-009-012022-01-28C16284748780-1d6a99b39-7c20-a426-e053-dadaa90af4c2afc83ddc-d2ce-1bbc-e053-2995a90a2b89
75035-010-012022-01-28C16284748780-1d6a99b39-7c20-a426-e053-dadaa90af4c2afc83ddc-d2ce-1bbc-e053-2995a90a2b89

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75035-009-01BYD Antibacterial Wet Wipes (Children)30 g in 1 BAGCLOTH301
75035-010-01BYD Antibacterial Wet Wipes (Children)30 g in 1 BAGCLOTH301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75035-009BYD ANTIBACTERIAL WET WIPES (CHILDREN) (DISINFECTANT WIPES) CLOTH [BYD AUTOMATIVE INDUSTRY CO., LTD.]1Legacy NDC, 1 package rows20200921_afc83ddc-d2ce-1bbc-e053-2995a90a2b89.zip
75035-010BYD ANTIBACTERIAL WET WIPES (CHILDREN) (DISINFECTANT WIPES) CLOTH [BYD AUTOMATIVE INDUSTRY CO., LTD.]1Legacy NDC, 1 package rows20200921_afc83ddc-d2ce-1bbc-e053-2995a90a2b89.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75035-00975035-009-01
75035-01075035-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
DECYL GLUCOSIDEZ17H97EA6YIACT
METHYLPARABENA2I8C7HI9TIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLPARABENZ8IX2SC1OHIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
METHYLPARABENA2I8C7HI9TIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLPARABENZ8IX2SC1OHIACT

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
afc83432-8fd6-6d2a-e053-2a95a90ae73fafc83ddc-d2ce-1bbc-e053-2995a90a2b892020-09-20WarningsExact identifier
spl id: afc83432-8fd6-6d2a-e053-2a95a90ae73f
spl set id: afc83ddc-d2ce-1bbc-e053-2995a90a2b89

Reported adverse events (FAERS/openFDA)#

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