FDA.reportPublic FDA data

Wet wipes

Manufacturer
Hangzhou Dijia Hygiene Products Co.,Ltd
Effective date
2020-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:07

Label at a glance#

ProductWet wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store below 110°F (43°C)

INACTIVE INGREDIENT SECTION

RO Pure Water,Glycerin, Propylene glycol, Phenoxyethanol,Didecyldimonium chloride

INDICATIONS & USAGE SECTION

●Wet hands thoroughly with product and allow to dry
●Children under 6 years of age should be supervised when using this wipe

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For external use only.When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a Doctor if iritation or rash appears and lasts.Keep out of reach of children. If swallowed, get medical help on contact a Poison Control Center right away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
87931-001-012022-11-16C16284748780-1d6a99b39-4455-a426-e053-dadaa90af4c2ab8b677b-29ff-e5e0-e053-2995a90a29f3
87931-001-012022-01-28C16284748780-1d6a99b39-4455-a426-e053-dadaa90af4c2ab8b677b-29ff-e5e0-e053-2995a90a29f3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87931-00187931-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT

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
ed926bec-2152-1ac3-e053-2a95a90ae243ab8b677b-29ff-e5e0-e053-2995a90a29f32022-11-16WarningsExact identifier
spl set id: ab8b677b-29ff-e5e0-e053-2995a90a29f3

Reported adverse events (FAERS/openFDA)#

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