RELIEF C ANTI-BACTERIAL FORMULA ANTI-BACTERIAL HAND SANITIZER- benzalkonium chloride liquid

Relief C Anti-Bacterial Formula Anti-Bacterial Hand Sanitizer by

Drug Labeling and Warnings

Relief C Anti-Bacterial Formula Anti-Bacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by FGD, LLC, Goodwin Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Directions

▪ Pump a small amount of foam into palm of hand

▪ Rub thoroughly over all surfaces of both hands for 15 seconds

▪ Rinse with potable water

Keep out of reach of children

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

Warnings

For external use only

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

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Uses

For hand washing to decrease bacteria on the skin

Recommended for repeated use

Inactive ingredients

Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid

Relief C Anti-Bacterial Formula Anti-Bacterial Hand Sanitizer

INGREDIENTS AND APPEARANCE

RELIEF C ANTI-BACTERIAL FORMULA ANTI-BACTERIAL HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73787-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73787-111-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/20/2020

Labeler - FGD, LLC (111927555)

Establishment
Name	Address	ID/FEI	Business Operations
Goodwin Co.		806987483	manufacture(73787-111)