FDA.reportPublic FDA data

WIPES

Manufacturer
Skaffles Group Limited Liability Company | Dalian Da Xin Nonwoven Technology Co.,Ltd.
Effective date
2020-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:50

Label at a glance#

ProductWIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Directions● Adults and children 2 yrs and over, apply to hands and allow skin to dry without wiping. ●Children under 2, ask doctor before use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USE

INDICATIONS & USAGE SECTION

Use for hand sanitizing to decrease bacteria on the skin
recommended for repeated use.

Warning

WARNINGS SECTION

For external use only. Do not use if you are allergic to
any of the ingredients.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions● Adults and children 2 yrs and over,
apply to hands and allow skin to dry without wiping.
●Children under 2, ask doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol,Sodium benzoate, Propylene glycol, Aloe barbadensis leaf juice, PEG-8 dimethicone, Disodium edta, Citric acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1812737benzalkonium Cl 0.3 % Medicated PadPSN1
1812737benzalkonium chloride 3 MG/ML Medicated PadSCD1
1812737benzalkonium chloride 0.3 % Medicated WipeSY1
1812737benzalkonium chloride 0.3 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77720-007-012022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-022022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-032022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-042022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-052022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-062022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-072022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE
77720-007-082022-01-28C16284748780-1d6a99b39-def2-a426-e053-dadaa90af4c277720-007 WIPES 0.3% BENZALKONIUM CHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77720-007-01WIPES1 in 1 BAGCLOTH11
77720-007-01WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-02WIPES15 in 1 POUCHCLOTH151
77720-007-02WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-03WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-03WIPES20 in 1 POUCHCLOTH201
77720-007-04WIPES25 in 1 POUCHCLOTH251
77720-007-04WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-05WIPES30 in 1 POUCHCLOTH301
77720-007-05WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-06WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-06WIPES50 in 1 POUCHCLOTH501
77720-007-07WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71
77720-007-07WIPES75 in 1 POUCHCLOTH751
77720-007-08WIPES100 in 1 POUCHCLOTH1001
77720-007-08WIPES2.7 g in 1 NOT APPLICABLECLOTH2.71

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77720-007WIPES (BENZALKONIUM CHLORIDE) CLOTH [SKAFFLES GROUP LIMITED LIABILITY COMPANY]1Legacy NDC, 16 package rows20200728_ab25ca2d-7758-1b02-e053-2a95a90a5a63.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77720-00777720-007-01, 77720-007-02, 77720-007-03, 77720-007-04, 77720-007-05, 77720-007-06, 77720-007-07, 77720-007-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PEG-8 DIMETHICONEGIA7T764ODIACT
DISODIUM EDTA-COPPER6V475AX06UIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
ab25c982-d5d5-d4d8-e053-2a95a90adc7aab25ca2d-7758-1b02-e053-2a95a90a5a632020-07-23WarningsExact identifier
spl id: ab25c982-d5d5-d4d8-e053-2a95a90adc7a
spl set id: ab25ca2d-7758-1b02-e053-2a95a90a5a63

Reported adverse events (FAERS/openFDA)#

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