AQUNOVA. WATER INNOVATION- hypochlorous acid liquid 
Agricultural Company Corporation, Inc

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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80542-201

ACTIVE INGREDIENTS

Hypochlorous Acid 0.1%

PURPOSE

Antiseptic

USES

Multi purpose sterilization, disinfection

WARNINGS

For external use only

When using this product

- Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

- Avoid contact with broken skin.

- Do not inhale or ingest.

WARNINGS

- Stop immediately and consult a doctor it you experience skin imitation or rash develops.

WARNINGS

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

DIRECTIONS

- Spray the sterilizing object in a wide range

- Please supervise when using the product by children, the elderly, the disabled, etc.

OTHER INFORMATION

- Read the directions and warmings before use

- If exposed to the air, sterilization may be reduced due to water-soluble, so keep the container sealed.

- Avoid freezing and excessive heat above 40 degreee C (104 degree F) 40C(104F)

INACTIVE INGREDIENTS

Water

PACKAGE LABEL

40ml NDC: 80542-201-01 Label

60ml NDC: 80542-201-02 Label

160ml NDC: 80542-201-03 Label

300ml NDC: 80542-201-04 Label

500ml NDC: 80542-201-05 Label

1000ml NDC: 80542-201-06 Label

3000ml NDC: 80542-201-07 Label

5000ml NDC: 80542-201-08 Label

10000ml NDC: 80542-201-09 Label

20000ml NDC: 80542-201-10 Label

AQUNOVA. WATER INNOVATION 
hypochlorous acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80542-201
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80542-201-0140 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/12/2020
2NDC:80542-201-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/12/2020
3NDC:80542-201-03160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/12/2020
4NDC:80542-201-04300 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
5NDC:80542-201-05500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
6NDC:80542-201-061000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
7NDC:80542-201-073000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
8NDC:80542-201-085000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
9NDC:80542-201-0910000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
10NDC:80542-201-1020000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/12/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/12/2020
Labeler - Agricultural Company Corporation, Inc (695005948)
Registrant - Agricultural Company Corporation, Inc (695005948)
Establishment
NameAddressID/FEIBusiness Operations
Agricultural Company Corporation, Inc695005948manufacture(80542-201)

Revised: 9/2020
Document Id: af151072-e3d7-64fe-e053-2a95a90a82c3
Set id: af151072-e3d6-64fe-e053-2a95a90a82c3
Version: 1
Effective Time: 20200911
 
Agricultural Company Corporation, Inc