BENZALKONIUM CHLORIDE INSTANT HAND SANITIZER- benzalkonium chloride instant hand sanitizer liquid 
Dongguan Mingyi Medical Products 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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74046-006
Benzalkonium Chloride Instant Hand Sanitizer

Active Ingredients

Benzalkotlm Chloide 0.13% v/v

​Purpose

Antiseptic

​Uses

Hand Sanitizer 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 eyas, 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.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing

Other Information

Store between 15-30℃ ( 59-86℉)

Avcid freezing and excessive heat above 40℃ ( 104℉)

Inactive Ingredients

aloe , glycerin , sterile distilled watet

Package Label - Principal Display Panel

74046-006-0174046-006-0274046-006-0374046-006-0474046-006-0574046-006-0674046-006-0774046-006-0874046-006-0974046-006-10

BENZALKONIUM CHLORIDE INSTANT HAND SANITIZER 
benzalkonium chloride instant hand sanitizer liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74046-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE (UNII: V5VD430YW9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74046-006-0110 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
2NDC:74046-006-0215 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
3NDC:74046-006-0320 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
4NDC:74046-006-0430 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
5NDC:74046-006-0540 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
6NDC:74046-006-0650 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
7NDC:74046-006-0760 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
8NDC:74046-006-08100 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
9NDC:74046-006-09250 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
10NDC:74046-006-10500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/15/2022
Labeler - Dongguan Mingyi Medical Products Co., Ltd. (554526907)
Registrant - Dongguan Mingyi Medical Products Co., Ltd. (554526907)
Establishment
NameAddressID/FEIBusiness Operations
Dongguan Mingyi Medical Products Co., Ltd.554526907manufacture(74046-006)

Revised: 3/2022
Document Id: d961c8c5-4453-5f0d-e053-2995a90a5a31
Set id: d5997471-55aa-4935-e053-2995a90a8cc0
Version: 5
Effective Time: 20220304
 
Dongguan Mingyi Medical Products Co., Ltd.