STERIL-WIZE ANTI-BACTERIAL FOAMING HAND- benzalkonium chloride soap
Nostalgia Products LLC

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.

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Steril-Wize Anti-Bacterial Foaming Hand Soap

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.

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, Glycerine, Caprylyl Glucoside, Tetrasodium EDTA, Benzisothiazol, Methylisothiazol, Fragrance, Citric Acid, Aloe Vera, Yellow #5, Red #40.

Package Labeling:946.35 mL

Bottle

Package Labeling:3.785L

Bottle2

STERIL-WIZE ANTI-BACTERIAL FOAMING HAND
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:77051-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
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)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:77051-001-32	946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2020
2	NDC:77051-001-37	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2020

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

Labeler - Nostalgia Products LLC (080132557)