JIKIMI PHYTONCIDE- titanium dioxide, hypochlorous acid liquid

JIKIMI Phytoncide by

Drug Labeling and Warnings

JIKIMI Phytoncide by is a Otc medication manufactured, distributed, or labeled by MY Corp.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hypochlorous Acid

INACTIVE INGREDIENT

Chamaecyparis Obtusa Leaf Extract, Foeniculum vulgare seed extract, Indican, Maltitol, Pinus Densiflora Leaf Extract, Sorbitol, Water

PURPOSE

• Do not dilute spray.
• Use at strength for maximum effectiveness.
• Spray directly, from a distance of about 8 to 10 inches.
• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Wipe with gauze or cotton swab and let air dry. Spray clothes, equipment, and indoor objects for sterilization and deodorization as required.

WARNINGS

For external use only.

When using this product

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

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

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

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

JIKIMI PHYTONCIDE 
titanium dioxide, hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71544-0020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.00136 g  in 17 mL

Inactive Ingredients
Ingredient Name	Strength
CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
INDICAN (UNII: N187WK1Y1J)
MALTITOL (UNII: D65DG142WK)
PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71544-0020-1	17 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/15/2020

Labeler - MY Corp.,Ltd (688202781)

Registrant - MY Corp.,Ltd (688202781)

Establishment
Name	Address	ID/FEI	Business Operations
MY Corp.,Ltd		688202781	manufacture(71544-0020) , label(71544-0020) , pack(71544-0020)