FDA.reportPublic FDA data

Penorra SANITARY WIPES

Manufacturer
Eastern Sources Inc
Effective date
2020-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:08

Label at a glance#

ProductPenorra SANITARY WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

• Hand sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

Unfold towelette: wipe hands, Discard after use.

Storage and handling

• Store between 15-30°C (59-86°F) • Avoid freezing and excessive heat above 40°C (104F) • May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only When using this product

• Do not use on open skin wounds

• 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

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

Directions

DOSAGE & ADMINISTRATION SECTION

Unfold towelette: wipe hands, Discard after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene glycol, Phenoxyethanol, Citric acid, Decyl glucoside, PHMB

Other information

STORAGE AND HANDLING SECTION

• Store between 15-30°C (59-86°F)

• Avoid freezing and excessive heat above 40°C (104F)

• May discolor certain fabrics or surfaces

Questions?

OTC - QUESTIONS SECTION

Sales@easternsourcesus.com

SPL UNCLASSIFIED SECTION

This product can effectively kill escherichia coli, staphylococcus aureus, candida albicans, etc

NO ALCOHOL

135 Route 59E

Spring Valley, NY 10977

Easternsourcesus.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78827-10278827-102-01, 78827-102-02, 78827-102-03, 78827-102-04, 78827-102-05, 78827-102-06, 78827-102-07, 78827-102-08, 78827-102-09, 78827-102-10, 78827-102-11, 78827-102-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
POLIHEXANIDE322U039GMFIACT

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
91bbf3bb-59b1-4923-8ec4-103f241c26c578c72d05-3dd5-4654-9473-bc32a548c5c92022-12-13WarningsExact identifier
spl set id: 78c72d05-3dd5-4654-9473-bc32a548c5c9

Reported adverse events (FAERS/openFDA)#

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