Wet Wipes

Manufacturer
Hangzhou Beitai Daily Commodity Co., Ltd.
Effective date
2020-09-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:09

Label at a glance#

ProductWet Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Storage and handling

/

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 hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use in the eyes

Stop use and ask a doctor if
irritation and redness develop
condition persists for, more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes

OTC - WHEN USING SECTION

Stop use and ask a doctor if
irritation and redness develop
condition persists for, more than 72 hours

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 and redness develop
condition persists for, more than 72 hours

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

wet hands thoroughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, EDTA disodium salt, phenoxyethanol, aloe vera leaf juice, tocopheryl acetate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

77765-015-01 35P77765-015-01 35P

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130789993962907GTIN-13: 0789993962907
EAN-13: 0789993962907
GTIN-12: 789993962907
UPC-A: 789993962907
GTIN storage (14 digits): 00789993962907
77765-015-01 35P.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77765-015-012022-01-28C16284748780-1d6a99b39-7b63-a426-e053-dadaa90af4c277765-015 Wet Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77765-015-01Wet Wipes35 in 1 DRUMCLOTH352

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77765-015WET WIPES (BENZALKONIUM WIPES) CLOTH [HANGZHOU BEITAI DAILY COMMODITY CO., LTD.]2Legacy NDC, 1 package rows20200912_af18d0e1-aae0-49ea-e053-2995a90a4960.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
77765-01577765-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
af18ff0a-581f-1706-e053-2995a90ab36faf18d0e1-aae0-49ea-e053-2995a90a49602020-09-12WarningsExact identifier
spl id: af18ff0a-581f-1706-e053-2995a90ab36f
spl set id: af18d0e1-aae0-49ea-e053-2995a90a4960

Reported adverse events (FAERS/openFDA)#

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