HYGENIX AF WIPE- benzalkonium chloride cloth

Hygenix AF Wipe by

Drug Labeling and Warnings

Hygenix AF Wipe by is a Otc medication manufactured, distributed, or labeled by GM Industrial, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BOXED WARNING

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Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1

Antiseptic

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of react of children

In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with product.

Discard wipe in trash receptacle after use. Do not flush.

Rub hands together briskly until dry.

Other information

Store in a cool dry place below 104 °F

Water, C9-11 Pareth-6, Cocamidopropyl PG-dimonium chloride phosphate, Dihydroxyethyl cocamine oxide, Acetamidoethoxyethanol, Citric acid.

PRINCIPAL DISPLAY PANEL

90 CT 74146-243-93

PRINCIPAL DISPLAY PANEL

74146-243-85

INGREDIENTS AND APPEARANCE

HYGENIX AF WIPE 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74146-243
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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74146-243-96	6 in 1 BOX	06/17/2021
1	NDC: 74146-243-93	647.3 mL in 1 CANISTER; Type 0: Not a Combination Product
2	NDC: 74146-243-86	4 in 1 BOX	06/17/2021
2	NDC: 74146-243-85	810.1 mL in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2021

Labeler - GM Industrial, Inc. (025827197)

Establishment
Name	Address	ID/FEI	Business Operations
GM Industrial, Inc.		025827197	manufacture(74146-243) , label(74146-243) , pack(74146-243) , relabel(74146-243) , repack(74146-243)