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Alegria Neo

Dosage form: paste, dentifrice
Ingredients: SILICON DIOXIDE 2.80g in 20g, Allantoin 0.008g in 20g
Labeler: Seowangmo Corporation
NDC Code: 70406-020

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.

ACTIVE INGREDIENT

Active Ingredient: Dental Type Silica 14.0%, Aluminium Chlorohydroxy Allantoinate 0.04%

INACTIVE INGREDIENT

Inactive Ingredients: D-Sorbitol Solution, Aqua, Polyethylene Glycol 1500, Mica, Concentrated Glycerin, Sodium Cocoyl Glutamate, Carboxymethylcellulose Sodium, Peppermint Oil, Anetol, Sophora Extract, Grapefruit Seed Extract, Xylitol, Glucosyl Stevia, L-Menthol, Hydroxyapatite, Eucalyptus Extract, Sage Extract, Chamomile Extract, Aloe Extract, Glycyrrhiza Extract Powder, Argentum

PURPOSE

Purpose: Gum Care

WARNINGS

Warnings: If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children: Keep out of reach of children under 6 years of age.

Use

Use: Aids in the prevention of gum care

Directions

Directions: 1) Adults and children 2 years of age and older: Brush teeth throughly preferably after each meal or at least twice a day or as directed by a dentist or doctor. 2) Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established. 3) Children under 2 years: Consult a dentist or doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ALEGRIA NEO 
silicon dioxide, allantoin paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70406-020
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE2.80 g  in 20 g
Allantoin (ALLANTOIN) Allantoin0.008 g  in 20 g
Inactive Ingredients
Ingredient NameStrength
WATER 
Xylitol 
Packaging
#Item CodePackage Description
1NDC:70406-020-021 TUBE in 1 CARTON
1NDC:70406-020-0120 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2017
Labeler - Seowangmo Corporation (689605288)
Registrant - Seowangmo Corporation (689605288)
Establishment
NameAddressID/FEIOperations
Seowangmo Corporation689605288manufacture(70406-020)

 
Seowangmo Corporation

Medically reviewed on Nov 3, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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