FDA.reportPublic FDA data

Sanitizing Wipes

Manufacturer
Imperial Palace Commodity (Shenzhen) Co., Ltd | Imperial Palace Commodity (Dongguan) Co., Ltd
Effective date
2020-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:34

Label at a glance#

ProductSanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

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 110F (43C). Dispose the used wipe in trash, do not flush it into the toilet. May discolor certain fabrics or surfaces.

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

For sanitizing and to help reduce bacteria on the skin. 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

  • in or near the eyes.
  • on open skin wounds or burns

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.

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

  • 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 110F (43C).
  • Dispose the used wipe in trash, do not flush it into the toilet.
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

cetylpyridinium chloride, chlorphenesin, propylene glycol, glycerol, water, ethylhexylglycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

800 PCS NDC: 71745-124-01800 PCS NDC: 71745-124-01

800 PCS NDC:52489-421-01

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
52489-421-012022-01-28C16284748780-1d6a99b39-6108-a426-e053-dadaa90af4c2Imperial-GoodEarth BZK Wipes 800 PCS
52489-421-022022-01-28C16284748780-1d6a99b39-6108-a426-e053-dadaa90af4c2Imperial-GoodEarth BZK Wipes 800 PCS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52489-421-01Sanitizing Wipes800 mL in 1 NOT APPLICABLESWAB8001
52489-421-01Sanitizing Wipes800 in 1 BAGSWAB8001
52489-421-02Sanitizing Wipes800 in 1 CANISTERSWAB8001
52489-421-02Sanitizing Wipes800 mL in 1 NOT APPLICABLESWAB8001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52489-421SANITIZING WIPES (WIPES) SWAB [IMPERIAL PALACE COMMODITY (SHENZHEN) CO., LTD]1Legacy NDC, 4 package rows20200917_af725aa9-de27-4245-e053-2a95a90ae1bb.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
52489-42152489-421-01, 52489-421-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORPHENESINI670DAL4SZIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT

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
af725aa9-de26-4245-e053-2a95a90ae1bbaf725aa9-de27-4245-e053-2a95a90ae1bb2020-09-16WarningsExact identifier
spl id: af725aa9-de26-4245-e053-2a95a90ae1bb
spl set id: af725aa9-de27-4245-e053-2a95a90ae1bb

Reported adverse events (FAERS/openFDA)#

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