AQUNOVA. WATER INNOVATION- hypochlorous acid liquid

AQUNOVA. WATER INNOVATION by

Drug Labeling and Warnings

AQUNOVA. WATER INNOVATION by is a Otc medication manufactured, distributed, or labeled by Agricultural Company Corporation, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

AQUNOVA. WATER INNOVATION 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80542-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80542-201-01	40 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/12/2020
2	NDC: 80542-201-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/12/2020
3	NDC: 80542-201-03	160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/12/2020
4	NDC: 80542-201-04	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
5	NDC: 80542-201-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
6	NDC: 80542-201-06	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
7	NDC: 80542-201-07	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
8	NDC: 80542-201-08	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
9	NDC: 80542-201-09	10000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020
10	NDC: 80542-201-10	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/12/2020

Labeler - Agricultural Company Corporation, Inc (695005948)

Registrant - Agricultural Company Corporation, Inc (695005948)

Establishment
Name	Address	ID/FEI	Business Operations
Agricultural Company Corporation, Inc		695005948	manufacture(80542-201)