G AND H PROTECT HAND- benzalkonium chloride soap 
Access Business Group LLC

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g&h Protect Hand Soap

Drug Facts

Active ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Uses

Helps reduce bacteria on hands.

Warnings

For external use only.

When using this product

avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor

if irritation develops. These may be signs of a serious condition.

Keep out of reach of children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wash hands and rinse.

Inactive ingredients:

Water, Cocamidopropyl Hydroxysultaine, Lauramidopropylamine Oxide, PEG-150 Distearate, Sodium Benzoate, Myristamidopropylamine Oxide, Lauramine Oxide, Citric Acid, Sodium Chloride, Glycerin, Fragrance, Tetrasodium EDTA, Propylene Glycol, Butylene Glycol, Ethanol, Aloe Barbadensis Leaf Juice, Dextrin, Centella Asiatica Extract, Camellia Sinensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Extract, Lecithin, Phenoxyethanol, Perilla Ocymoides Leaf Extract, Ceramide NP, Beta-Sitosterol, Chlorphenesin, Potassium Sorbate, Tocopherol

Questions?

USA: 1-800-253-6500

Package Labeling:

Label0

G AND H PROTECT HAND 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10056-026
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
EDETATE SODIUM (UNII: MP1J8420LU)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
ROSEMARY (UNII: IJ67X351P9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)  
CERAMIDE NP (UNII: 4370DF050B)  
.BETA.-SITOSTEROL (UNII: S347WMO6M4)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10056-026-00250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)04/19/2023
Labeler - Access Business Group LLC (839830713)

Revised: 10/2023
Document Id: 085c311d-9905-e891-e063-6394a90aae95
Set id: 1103a4af-10d6-478f-85cd-c364569569e5
Version: 2
Effective Time: 20231023
 
Access Business Group LLC