G AND H PROTECT HAND- benzalkonium chloride soap

g and h Protect Hand by

Drug Labeling and Warnings

g and h Protect Hand by is a Otc medication manufactured, distributed, or labeled by Access Business Group LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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:

INGREDIENTS AND APPEARANCE

G AND H PROTECT HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10056-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10056-026-00	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/19/2023

Labeler - Access Business Group LLC (839830713)