FDA.reportPublic FDA data

BODY WIPE

Manufacturer
ZheJiang HuaShun Technology Co.,Ltd
Effective date
2024-03-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:07:43

Label at a glance#

ProductBODY WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

to maximize efectiveness,use a different side on each body part.Allow skin to air dry.Do not flush.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, wipe

Use

INDICATIONS & USAGE SECTION

decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.if contact occurs,rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.

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 appear

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

to maximize efectiveness,use a different side on each body part.Allow skin to air dry.Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water,aloe barbadensis leaf juice,citric acid，fragrance,glycerin,hamamelis virginiana(witch hazel) bark/leaf/twig extract,phenoxyethanol,polysibate 20,tocopheryl acetate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77046-005-012024-03-18C16284748780-1d6a99b39-90a3-a426-e053-dadaa90af4c2aa4ac3ce-d5d4-7a5d-e053-2995a90a6814
77046-005-012024-01-30C16284748780-1d6a99b39-90a3-a426-e053-dadaa90af4c2aa4ac3ce-d5d4-7a5d-e053-2995a90a6814
77046-005-012022-12-06C16284748780-1d6a99b39-90a3-a426-e053-dadaa90af4c2aa4ac3ce-d5d4-7a5d-e053-2995a90a6814
77046-005-012022-01-28C16284748780-1d6a99b39-90a3-a426-e053-dadaa90af4c2aa4ac3ce-d5d4-7a5d-e053-2995a90a6814

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
77046-00577046-005-01

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
DECYL GLUCOSIDEZ17H97EA6YIACT
ALOEV5VD430YW9IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
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
2b3dcae1-24f6-4a95-e063-6294a90a55bfaa4ac3ce-d5d4-7a5d-e053-2995a90a68142025-01-08WarningsExact identifier
spl set id: aa4ac3ce-d5d4-7a5d-e053-2995a90a6814

Reported adverse events (FAERS/openFDA)#

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