DONE HAND ANTIBACTERIAL FRUITY FUSION- benzalkonium chloride liquid

Done Hand Antibacterial Fruity Fusion by

Drug Labeling and Warnings

Done Hand Antibacterial Fruity Fusion by is a Otc medication manufactured, distributed, or labeled by Olein Recovery Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial 

Use

for handwashing to decrease bacteria on ths skin.

Warnings

For external use only

When using this product,

avoid contact with eyes. In case of contact flush with water.

Stop use and ask a doctor if

irritation and redness develops.

Keep out of reach of children.

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

Directions 

wash skin, rinse and dry thoroughly

Inactive ingredients

purified water, sodium laureth sulfate, sodium C14-16 olefin sulfonate, cocamidorpyopyl betaine, sodium chloride, glycerine, fragrance, tetrasodium EDTA, methylchloroisothiazolinone, Methylisothiazolinone, D&C orange No.4

Package Labeling: Done Hand Soap Antibacterial Fruity Fusion, 296,mL

INGREDIENTS AND APPEARANCE

DONE HAND ANTIBACTERIAL FRUITY FUSION 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77142-009
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)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77142-009-00	296 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/15/2020

Labeler - Olein Recovery Corporation (188543446)