VITAPLUS FORE- ethanol, titanium dioxide liquid 
MY Corp.,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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Ethanol, Titanium Dioxide

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

Antiseptic

keep out of reach of the children

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

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.

for external use only

1

VITAPLUS FORE 
ethanol, titanium dioxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71544-0022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.008 g  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.01 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)  
INDICAN (UNII: N187WK1Y1J)  
SORBITOL (UNII: 506T60A25R)  
MALTITOL (UNII: D65DG142WK)  
WATER (UNII: 059QF0KO0R)  
FENNEL SEED (UNII: G3QC02NIE6)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71544-0022-14000 mL in 1 DRUM; Type 0: Not a Combination Product04/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2021
Labeler - MY Corp.,Ltd (688202781)
Registrant - MY Corp.,Ltd (688202781)
Establishment
NameAddressID/FEIBusiness Operations
MY Corp.,Ltd688202781manufacture(71544-0022) , label(71544-0022) , pack(71544-0022)

Revised: 4/2021
Document Id: c00e83d3-9980-2bfc-e053-2a95a90a7bab
Set id: bfe9c7fd-1e43-627d-e053-2a95a90ae03c
Version: 2
Effective Time: 20210415
 
MY Corp.,Ltd