ANZOON ANTISEPTIC WIPES- benzethonium chloride/benzalkonium chloride cloth

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredient

Benzethonium Chloride 0.05%

Benzalkonium Chloride 0.05%

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only

When using this product

Do not use on open skin wounds

Do not use

Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

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

Unfold towelette: wipe hands, Discard after use

Inactive ingredients

Propylene Glycol

Lodopropynyl Butylcarbanate

Glycerin

Water

Other information

Store between 15-30 °C(59-86°F)

Do not store above 110 °F (43°C)

label

INGREDIENTS AND APPEARANCE

ANZOON ANTISEPTIC WIPES 
benzethonium chloride/benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87638-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.05 g  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87638-001-01	1 in 1 CONTAINER	04/27/2026
1		10 mL in 1 CONTAINER; Type 0: Not a Combination Product
2	NDC: 87638-001-02	10 in 1 CONTAINER	04/27/2026
2		100 mL in 1 CONTAINER; Type 0: Not a Combination Product
3	NDC: 87638-001-03	20 in 1 CONTAINER	04/27/2026
3		200 mL in 1 CONTAINER; Type 0: Not a Combination Product
4	NDC: 87638-001-04	30 in 1 CONTAINER	04/27/2026
4		300 mL in 1 CONTAINER; Type 0: Not a Combination Product
5	NDC: 87638-001-05	50 in 1 CONTAINER	04/27/2026
5		500 mL in 1 CONTAINER; Type 0: Not a Combination Product
6	NDC: 87638-001-06	80 in 1 CONTAINER	04/27/2026
6		800 mL in 1 CONTAINER; Type 0: Not a Combination Product
7	NDC: 87638-001-07	100 in 1 CONTAINER	04/27/2026
7		1000 mL in 1 CONTAINER; Type 0: Not a Combination Product
8	NDC: 87638-001-08	500 in 1 CONTAINER	04/27/2026
8		5000 mL in 1 CONTAINER; Type 0: Not a Combination Product
9	NDC: 87638-001-09	800 in 1 CONTAINER	04/27/2026
9		8000 mL in 1 CONTAINER; Type 0: Not a Combination Product
10	NDC: 87638-001-10	1000 in 1 CONTAINER	04/27/2026
10		10000 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/27/2026

Labeler - Shandong ACZ Biotechnology Co., Ltd. (844599612)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong AZC Biotechnology Co.,Ltd.		844599612	manufacture(87638-001)