Zogics Antibacterial Hand by Zogics, LLC

Zogics Antibacterial Hand by

Drug Labeling and Warnings

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

Drug Details [pdf]

ZOGICS ANTIBACTERIAL 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 Lauryl Sulfate (68585-47-7), Cocamidopropyl Hydroxysultaine (68139-30-0), Sodium Chloride (7647-14-5), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycol Distearate (627-83-8), Fragrance (Proprietary), Sodium Citrate (6132-04-3), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4), 2-Bromo-2- Nitropropane-1,3-Diol (52-51-7).

ZOGICS ANTIBACTERIAL HAND 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72202-301
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
BRONOPOL (UNII: 6PU1E16C9W)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
PROPANEDIOL (UNII: 5965N8W85T)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72202-301-41	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/15/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/15/2024	10/31/2025

Labeler - Zogics, LLC (796321870)

Revised: 1/2026

Document Id: 48c366e5-e4df-d655-e063-6394a90a809f

34390-5

Set id: 13b2c1f5-c04f-daa7-e063-6394a90a83b3

Version: 4

Effective Time: 20260119