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 21:28:39

Label at a glance#

ProductSIPA HAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE, ALCOHOL
Label structure6 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Discard wipes in trash receptacles 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%

Alcohol 4%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

Muli-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 use and ask a doctor if irritation or rash appears and lasts.

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 receptacles 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, Decy Glucoside, Glycerin, Ehtylhe xylglycerin, 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-130040232528965GTIN-13: 0040232528965
EAN-13: 0040232528965
GTIN-12: 040232528965
UPC-A: 040232528965
GTIN storage (14 digits): 00040232528965		SIPA HAND SANITIZING WIPES 50 pcs.jpg

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
78823-05078823-050-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALCOHOL3K9958V90MACTIB
water059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
DECYL GLUCOSIDEZ17H97EA6YIACT

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
1bc2a091-6675-e8b5-e063-6294a90ac23885586c31-8913-41c4-9c06-a75bb08f3a422024-06-25WarningsExact identifier
spl set id: 85586c31-8913-41c4-9c06-a75bb08f3a42

Reported adverse events (FAERS/openFDA)#

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