VITAPLUS FORE- ethanol, titanium dioxide liquid

Vitaplus fore by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Ethanol, Titanium Dioxide

INACTIVE INGREDIENT

Pinus densiflora callus extract ,Foeniculum vulgare seed extract,Indican,Maltitol,Sorbitol,Water

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Do not dilute. Use at strength for maximum effectiveness. For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

WARNINGS

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 ifirritation 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

VITAPLUS FORE 
ethanol, titanium dioxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71544-0022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.008 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.01 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
INDICAN (UNII: N187WK1Y1J)
SORBITOL (UNII: 506T60A25R)
MALTITOL (UNII: D65DG142WK)
WATER (UNII: 059QF0KO0R)
FENNEL SEED (UNII: G3QC02NIE6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71544-0022-1	4000 mL in 1 DRUM; Type 0: Not a Combination Product	04/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2021

Labeler - MY Corp.,Ltd (688202781)

Registrant - MY Corp.,Ltd (688202781)

Establishment
Name	Address	ID/FEI	Business Operations
MY Corp.,Ltd		688202781	manufacture(71544-0022) , label(71544-0022) , pack(71544-0022)