MUNDUS HYPOCHLOROUS ACID HAND SANITIZER- mundus hypochlorous acid hand sanitizer liquid 
Jiacheng Tech (Zhejiang) Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Mundus Hypochlorous Acid Hand Sanitizer
55683-002-01 480ml
55683-002-02 100ml
55683-002-03 25L
55683-002-04 10L
55683-002-05 60ml
55683-002-06 80ml
55683-002-07 300ml
55683-002-08 500ml

Active Ingredient(s)

Hypochlorous acid 0.015%

Purpose

Antiseptic, Hand Sanitizer

Use

Used to wash hands to help reduce bacteria that potentially can cause disease.

Warnings

Do not use

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, ger medical help or contact a poison control center right away.

Directions

Other information

Inactive ingredients

Hypochlorite Ion, Sodium Chloride(Salt), lonized Water.

Package Label - Principal Display Panel

480 mL NDC: 55683-003-01 480mL label

100 mL NDC: 55683-003-02 100mL label

25000 mL NDC: 55683-003-03 25000mL label

10000 mL NDC: 55683-003-04 10000mL label

60 mL NDC: 55683-003-05 60mL label

80 mL NDC: 55683-003-06 80mL label

300 mL NDC: 55683-003-07 300mL label

500 mL NDC: 55683-003-08 500mL label

MUNDUS HYPOCHLOROUS ACID HAND SANITIZER 
mundus hypochlorous acid hand sanitizer liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55683-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.015 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYPOCHLORITE ION (UNII: T5UM7HB19N)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55683-003-01480 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
2NDC:55683-003-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
3NDC:55683-003-0325000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
4NDC:55683-003-0410000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
5NDC:55683-003-0560 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
6NDC:55683-003-0680 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
7NDC:55683-003-07300 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
8NDC:55683-003-08500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/22/2020
Labeler - Jiacheng Tech (Zhejiang) Co., Ltd. (554548070)
Establishment
NameAddressID/FEIBusiness Operations
Jiacheng Tech (Zhejiang) Co., Ltd.554548070manufacture(55683-003)

Revised: 3/2022
Document Id: da2dd2c7-e5a8-da22-e053-2a95a90a5571
Set id: b23b19a9-b060-49b1-e053-2a95a90aef2e
Version: 4
Effective Time: 20220314
 
Jiacheng Tech (Zhejiang) Co., Ltd.