FDA.reportPublic FDA data

SIPA HAND SANITIZING WIPES

Manufacturer
Zhejiang Ruolin Hygienic Products Co., Ltd.
Effective date
2023-07-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:28:38

Label at a glance#

ProductSIPA HAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Discard wipes in trash receptacle after use. Do not flush. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Multi-purpose cleaning and hand sanitizing

Warning

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 using and ask a doctor if irritation or rash appears and lasts 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Contrl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Discard wipes in trash receptacle after use. Do not flush.
  • Children under 6 years of age should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Decyl glucoside, Glycerin, Ehtylhexylglycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Parfum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label imagelabel image

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130040232498732GTIN-13: 0040232498732
EAN-13: 0040232498732
GTIN-12: 040232498732
UPC-A: 040232498732
GTIN storage (14 digits): 00040232498732		SIPA HAND SANITIZING WIPES 100 250 500 pcs.jpg

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
78823-05178823-051-01, 78823-051-02, 78823-051-03

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
water059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
1bc26bbe-e698-7156-e063-6294a90a6c8c624bcae8-e21b-4618-a6cc-3c971575d2882024-06-25WarningsExact identifier
spl set id: 624bcae8-e21b-4618-a6cc-3c971575d288

Reported adverse events (FAERS/openFDA)#

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