Sanitx Wet Wipes

Manufacturer
SANITA PERSONA SAL
Effective date
2020-07-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:21:49

Label at a glance#

ProductSanitx Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingedient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use if you are allergic to any of the ingredients

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin.

Stop use and ask a doctor if irritation or redness develops and the condition persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Propylene glycol, Polyquaternium-7, Phenoxyethanol, PEG-7 Glyceryl Cocoate, Polysorbate-20, Parfum, Aloe Barbadensis Leaf Extract, Urea, Ethylenediaminetetraacetic acid, Tetrasodium salt, Ethylhexylglycerin, Methylisothiazolinone

Sanitx Wet Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1234.jpg1234.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130854145008656GTIN-13: 0854145008656
EAN-13: 0854145008656
GTIN-12: 854145008656
UPC-A: 854145008656
GTIN storage (14 digits): 00854145008656
1234.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78822-100-022022-01-28C16284748780-1d6a99b39-c51c-a426-e053-dadaa90af4c2Sanitx Wet Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78822-100-01Sanitx Wet Wipes10 in 1 POUCHLIQUID104
78822-100-02Sanitx Wet Wipes4 in 1 PACKAGELIQUID44

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78822-100SANITX WET WIPES (BENZALKONIUM CHLORIDE) LIQUID [SANITA PERSONA SAL]4Legacy NDC, 2 package rows20200718_a7af5dad-2bd4-717e-e053-2995a90aafeb.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78822-10078822-100-01, 78822-100-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
aaad2414-51de-9292-e053-2a95a90add09a7af5dad-2bd4-717e-e053-2995a90aafeb2020-07-17WarningsExact identifier
spl id: aaad2414-51de-9292-e053-2a95a90add09
spl set id: a7af5dad-2bd4-717e-e053-2995a90aafeb

Reported adverse events (FAERS/openFDA)#

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