The Home Edit Antibacterial Hand Wash-Unscented by LAB-CLEAN, INC

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]

THE HOME EDIT ANTIBACTERIAL HAND WASH-UNSCENTED- benzalkonium chloride liquid 
LAB-CLEAN, INC

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.

----------

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 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. 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

Label

THE HOME EDIT ANTIBACTERIAL HAND WASH-UNSCENTED 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73126-029
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73126-029-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
2NDC: 73126-029-02450 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
3NDC: 73126-029-03474 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
4NDC: 73126-029-04502 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
5NDC: 73126-029-05532 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
6NDC: 73126-029-06710 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
7NDC: 73126-029-07946 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/01/202004/20/2024
Labeler - LAB-CLEAN, INC (199822219)
Establishment
NameAddressID/FEIBusiness Operations
LAB-CLEAN, INC199822219manufacture(73126-029)

Revised: 4/2022
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.