MYREMEDE SANITIZING WIPES- benzalkonium chloride cloth

MyRemede Sanitizing Wipes by

Drug Labeling and Warnings

MyRemede Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Remede Organics, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use

Sanitizing wipes designed to help reduce bacteria when soap and water are not available or practical.

Warnings

For external use only. For single and non-medical use only. Appropriately dispose of used wipes.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and consult a doctor if

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If ingested, get medical help or contact a Poison Control Center right away.

Directions

• Apply topicall as needed to intended surfaces. Let air dry.
• Supervise children under 6 years of age when using this product to avoid choking.
• Please keep sealed between uses to maintain adequate moisture.
• Do not flush wipes.

Other Information

Store at room temperature.

Inactive Ingredients

Pure water, Didecyldimethylammonium chloride, 2-Phenoxyethanol, 3-[2-(Ethylhexyloxy]-1,2-propanediol, 1,2-Propanediol, Glycerol

Package Labeling:

INGREDIENTS AND APPEARANCE

MYREMEDE SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77529-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77529-001-50	50 in 1 PACKAGE	07/10/2020
1		4.728 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/10/2020

Labeler - Remede Organics, Inc (117506657)