Zogics Antibacterial Foaming Hand by Zogics, LLC

Zogics Antibacterial Foaming Hand by

Drug Labeling and Warnings

Zogics Antibacterial Foaming Hand by is a Otc medication manufactured, distributed, or labeled by Zogics, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ZOGICS ANTIBACTERIAL FOAMING HAND- chloroxylenol soap 
Zogics, LLC

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ACTIVE INGREDIENT

Chloroxylenol 0.1%

PURPOSE

Antiseptic Handwashing

USES

Handwash to help decrease bacteria on the skin.

WARNINGS

For external use only.
Do not use in the eyes. In case of contact, immediately flush eyes with water.

Stop use and ask a doctor if irritation or rash appears and lasts

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly.
Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENTS

Water (Aqua) (7732-18-5), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycerin (56-81-5), Cocamidopropyl Hydroxysultaine (68139-30-0), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium Polyitaconate (26099-89-8), Dibromocyanoacetamide (10222-01-2), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4)

ZOGICS ANTIBACTERIAL FOAMING HAND 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72202-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	1 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED) (UNII: G7SW5QN7TT)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPANEDIOL (UNII: 5965N8W85T)
BRONOPOL (UNII: 6PU1E16C9W)
GLYCERIN (UNII: PDC6A3C0OX)
DIBROMOCYANOACETAMIDE (UNII: 7N51QGL6MJ)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72202-201-41	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/14/2024	01/30/2026

Labeler - Zogics, LLC (796321870)

Revised: 7/2025

Document Id: 3b00a75f-6a2a-5259-e063-6394a90af1ff

34390-5

Set id: 13a4fd19-648c-88d8-e063-6294a90a0370

Version: 3

Effective Time: 20250728