THE HOME EDIT ANTIBACTERIAL HAND WASH-UNSCENTED- benzalkonium chloride liquid

The Home Edit Antibacterial Hand Wash-Unscented by

Drug Labeling and Warnings

The Home Edit Antibacterial Hand Wash-Unscented by is a Otc medication manufactured, distributed, or labeled by LAB-CLEAN, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

For hand Sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only.

WHEN USING

• When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.
• Do not ingest.
• Stop use and ask a doctor if irritation or redness develops and conditions persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Apply small amount of product to wet hands. Work into lather and rinse thoroughly. Dry hands.

Inactive ingredients

Water, Cocamidopropyl Betaine, PEG-150 Distearate, Caprylyl Glucoside, Glycerine, Cocamide MIPA, Tetrasodium EDTA, Citric Acid, Aloe Vera, Benzisothiazol, Methylisathiozol.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

THE HOME EDIT ANTIBACTERIAL HAND WASH-UNSCENTED 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73126-029
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)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
GLYCERIN (UNII: PDC6A3C0OX)
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73126-029-01	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
2	NDC: 73126-029-02	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
3	NDC: 73126-029-03	474 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
4	NDC: 73126-029-04	502 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
5	NDC: 73126-029-05	532 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
6	NDC: 73126-029-06	710 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020
7	NDC: 73126-029-07	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/01/2020	04/20/2024

Labeler - LAB-CLEAN, INC (199822219)

Establishment
Name	Address	ID/FEI	Business Operations
LAB-CLEAN, INC		199822219	manufacture(73126-029)