GOOD TO GO ANTIBACTERIAL HAND WIPES- benzalkonium chloride swab

Good to Go Antibacterial Hand Wipes by

Drug Labeling and Warnings

Good to Go Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Navajo Manufacturing Company Inc., Kangna (Zhejiang) Medical Supplies Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.3%

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develops

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

Directions

• Take wipe and rub thoroughly over all surfaces of both hands.
• Rub hands together briskly to dry.
• Dispose of wipe.

Inactive ingredients

Water, Phenoxyethanol, DMDM Hydantoin, Ethylparaben, Methylparaben, Polysorbate 20, Fragrance, Disodium EDTA, Sodium Citrate, Cetylpyridinium Chloride.

Package Label

INGREDIENTS AND APPEARANCE

GOOD TO GO ANTIBACTERIAL HAND WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67751-210
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLPARABEN (UNII: 14255EXE39)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Product Characteristics
Color		Score
Shape		Size
Flavor	LEMON	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67751-210-50	50 in 1 POUCH	01/25/2021
1		136.5 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/25/2021	11/01/2022

Labeler - Navajo Manufacturing Company Inc. (091917799)

Establishment
Name	Address	ID/FEI	Business Operations
Kangna (Zhejiang) Medical Supplies Co., Ltd.		554530173	manufacture(67751-210) , label(67751-210)