DISINFECTING WIPES by Hangzhou Muzi Commodity Co., Ltd DISINFECTING WIPES

DISINFECTING WIPES by

Drug Labeling and Warnings

DISINFECTING WIPES by is a Otc medication manufactured, distributed, or labeled by Hangzhou Muzi Commodity Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DISINFECTING WIPES- benzalkonium chloride solution 
Hangzhou Muzi Commodity Co., Ltd

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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DISINFECTING WIPES

DISINFECTING WIPES

Active Ingredient(s)

BENZALKONIUM CHLORIDE 0.0052mg/pcs. Purpose: Antiseptic

Purpose

Antiseptic, DISINFECTING WIPES

Use

DISINFECTING WIPES to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands thoroghly with product and allow to dry.
• Discard wipes in trash receptacle after use. Do not flush.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Aloe Barbadensis Leaf Juice
Fragrance
Phenoxyethanol
Polysorbate 20
Propylene Glycol
Tocopheryl Acetata
Water

Package Label - Principal Display Panel

DISINFECTING WIPES 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80707-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0052 mg

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80707-101-01	35 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 80707-101-02	40 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 80707-101-03	50 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 80707-101-04	60 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 80707-101-05	70 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 80707-101-06	75 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 80707-101-07	80 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 80707-101-08	90 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
9	NDC: 80707-101-09	100 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
10	NDC: 80707-101-10	120 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
11	NDC: 80707-101-11	150 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
12	NDC: 80707-101-12	160 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
13	NDC: 80707-101-13	180 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
14	NDC: 80707-101-14	200 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
15	NDC: 80707-101-15	250 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
16	NDC: 80707-101-16	300 in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020	12/17/2020

Labeler - Hangzhou Muzi Commodity Co., Ltd (554551057)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Muzi Commodity Co., Ltd		554551057	manufacture(80707-101)

Revised: 12/2020

Document Id: b6a5173d-4af5-3ab3-e053-2a95a90ac4b5

34390-5

Set id: b0990081-15fb-2cff-e053-2a95a90a7ca0

Version: 2

Effective Time: 20201217