Sanitized Pro Multi-Purpose Antibacterial Wipes

Manufacturer
Poseidon Technology, LLC
Effective date
2020-09-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:55

Label at a glance#

ProductSanitized Pro Multi-Purpose Antibacterial Wipes
Active ingredientHYPOCHLOROUS ACID
Label structure14 sections

Dosage and administration

Adults and children 2 years and over: Apply to area and allow to dry without wiping. Children should be supervised when using and those under 2 years of age ask doctor before use. Do not flush. Discard in a trash receptacle.

Storage and handling

Storage - Keep containers tightly closed to keep wipes from drying out. Keep out of sunlight and store in a cool place.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

  1. Hypochlorous Acid
  2. Sodium Chloride
  3. Water.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION


Hypochlorous Acid (EPA Reg# 96048-1)...........Sanitizing/Antimicrobial Agent
Solution is on the EPA N-List N-Products with Emerging Viral Pathogens and
Human Coronavirus claims for use against SARS CoV-2.

Purpose

OTC - PURPOSE SECTION

Sanitizing/Antimicrobial Agent

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to the ingredient. Avoid contact to the
eyes and skin. May irritate eyes or sensitive skin. If contact occurs rinse
thoroughly with water.

OTC - WHEN USING SECTION

Avoid contact of eyes and skin at full strength may irritate eyes or sensitive skin. In case of eye contact immediately flush eyes with plenty of fresh water. If skin irritation occurs, wash with soap and water.

OTC - STOP USE SECTION

If irritation or rash develops and
continues for more than 72hrs.

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

Adults and children 2 years and over: Apply to area and
allow to dry without wiping. Children should be supervised when using and
those under 2 years of age ask doctor before use. Do not flush. Discard in a
trash receptacle.

Other information

STORAGE AND HANDLING SECTION

Storage - Keep containers tightly closed to keep wipes from drying out.
Keep out of sunlight and store in a cool place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water and Sodium Chloride

RECENT MAJOR CHANGES SECTION

Decreases bacteria on skin.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package.Label Principal Display PanelPackage.Label Principal Display PanelPackage.Label Principal Display PanelPackage.Label Principal Display PanelPackage.Label Principal Display PanelPackage.Label Principal Display Panel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80546-001-16Sanitized Pro Multi-Purpose Antibacterial Wipes800 g in 1 CANISTERCLOTH8002
80546-001-50Sanitized Pro Multi-Purpose Antibacterial Wipes2500 g in 1 CANISTERCLOTH25002
80546-001-80Sanitized Pro Multi-Purpose Antibacterial Wipes400 g in 1 CANISTERCLOTH4002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80546-001SANITIZED PRO MULTI-PURPOSE ANTIBACTERIAL WIPES (WIPES) CLOTH [POSEIDON TECHNOLOGY, LLC]2Legacy NDC, 3 package rows20200923_af09c081-a819-da13-e053-2a95a90a317b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80546-00180546-001-80, 80546-001-16, 80546-001-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB
SODIUM CHLORIDE451W47IQ8XIACT

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
afeb1427-0861-ba03-e053-2a95a90a79fcaf09c081-a819-da13-e053-2a95a90a317b2020-09-22WarningsExact identifier
spl id: afeb1427-0861-ba03-e053-2a95a90a79fc
spl set id: af09c081-a819-da13-e053-2a95a90a317b

Reported adverse events (FAERS/openFDA)#

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