SANITIZED PRO MULTI-PURPOSE ANTIBACTERIAL WIPES- wipes cloth

Sanitized Pro Multi-Purpose Antibacterial Wipes by

Drug Labeling and Warnings

Sanitized Pro Multi-Purpose Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Poseidon Technology, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

Active Ingredient(s)

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

Sanitizing/Antimicrobial Agent

Use

Decreases bacteria on skin.

Warnings

For external use only.

Do not use

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.

WHEN USING

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.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

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

Inactive ingredients

Water and Sodium Chloride

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SANITIZED PRO MULTI-PURPOSE ANTIBACTERIAL WIPES 
wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80546-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)	16.26 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80546-001-80	400 g in 1 CANISTER; Type 0: Not a Combination Product	03/30/2020
2	NDC: 80546-001-16	800 g in 1 CANISTER; Type 0: Not a Combination Product	03/30/2020
3	NDC: 80546-001-50	2500 g in 1 CANISTER; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/30/2020

Labeler - Poseidon Technology, LLC (103470197)

Registrant - Poseidon Technology, LLC (103470197)

Establishment
Name	Address	ID/FEI	Business Operations
Poseidon Technology, LLC		103470197	manufacture(80546-001)