STERIL WIZE ANTI BACTERIAL LIQUID HAND- benzalkonium chloride soap

Steril Wize Anti Bacterial Liquid Hand by

Drug Labeling and Warnings

Steril Wize Anti Bacterial Liquid Hand by is a Otc medication manufactured, distributed, or labeled by Nostalgia Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride .13%

Purpose

Antiseptic

Uses

• For handwashing to decrease bacteria on the skin.

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 persist for more than 72 hours.

Keep out of reach of children.

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

Directions

• Apply soap into hands, wet as needed 
• Lather vigorously for at least 15 seconds · Wash skin, rinse thoroughly and dry.

Inactive Ingredients

Water,Cocamidopropyl Betaine, PEG 150 Distearate, Caprylyl Glucoside, Glycerine, Cacomide PAMMI, Tetrasodium EDTA, Fragrance, Citric Acid, Aloe Vera, Benzisothiazol, Methylisothiazol, Yellow #5, Red #40.

Package Labeling:

INGREDIENTS AND APPEARANCE

STERIL WIZE ANTI BACTERIAL LIQUID HAND 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77051-002
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)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77051-002-32	946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/16/2020

Labeler - Nostalgia Products LLC (080132557)