GD Disinfectant Wipes by JRB Group dba/ Grand Destiny Group GD Disinfectant Wipes

GD Disinfectant Wipes by

Drug Labeling and Warnings

GD Disinfectant Wipes by is a Otc medication manufactured, distributed, or labeled by JRB Group dba/ Grand Destiny Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GD DISINFECTANT WIPES- benzalkonium chloride cloth 
JRB Group dba/ Grand Destiny Group

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

GD Disinfectant Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride(0.13%)

Purpose

Antibacterial

Uses:

For sanitizing and to help reduce bacteria on the skin

Warnings:

Do not use

if you are allergic to any of the ingredients.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away. For external use only.

Directions:

Open the lid and tear off the inner seal. Gently pull out the wipe. Thoroughly wip the skin as desired. Dispose of the used wipe in the trash, do not flush it into the toilet.

Inactive Ingredients:

Water, Phenoxyethanol, Sodium benzoate, Propylene glycol, Aloe barbadensis leaf juice, PEG-8 dimethicone, Disodium EDTA, Citric acid.

Package Labeling:50 Wipes

Package Labeling:80 Wipes

GD DISINFECTANT WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81166-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81166-000-50	50 in 1 BAG	12/30/2020	09/30/2021
1		3.96 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 81166-000-80	80 in 1 BAG	12/30/2020	09/30/2021
2		3.96 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	12/30/2020	09/30/2021

Labeler - JRB Group dba/ Grand Destiny Group (120975118)

Revised: 10/2021

Document Id: cf4294a0-c6ab-09ef-e053-2995a90a8eb7

34390-5

Set id: b6225859-b7fa-e328-e053-2a95a90a5793

Version: 2

Effective Time: 20211026