Newchito Plus One description, usages, side effects, indications, overdosage, supplying and lots more!

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Newchito Plus One

Sungwon Pharmaceutical Co., Ltd.
Sungwon Pharmaceutical Co., Ltd.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient

SODIUM MONOFLUOROPHOSPHATE   0.66%


Purpose

Purpose

Anticavity

Warning

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

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

Uses

Direction

adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician
children 2 to 6 years use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
children under 2 years ask a dentist or physician

Brush your teeth at least twice a day preferably after each meal

Use two pea sized amount for adult and one pea sized amount for children (age 2 to 6) and brushing and rinsing mouth

Inactive Ingredient

Colloidal silicon Dioxide
Tribasic Calcium Phosphate 
Chitosan
Xylitol
L-Menthol
steviol glycoside
Sodium Lauryl Sulfate
Dionized Water
Glycerine
D-sorbitol Solution
Sodium Carboxymethylcellulose
Alkyl(8-16) glcoside
Polyethylenglycol 4000
Peppermint oil
Calendura extract
Licorice Extract
Moutan Root bark Extract
Grapefruit seed extract
Perilla herb extract
Propolis extract

Newchito Plus OneEnter section text here

Newchito Plus One

SODIUM MONOFLUOROPHOSPHATE PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76058-101
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 1452 mg

Inactive Ingredients

Ingredient Name Strength
CALCIUM CARBONATE
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
ALUMINUM
AMINOCAPROIC ACID
CHITOSAN LOW MOLECULAR WEIGHT (20-200 MPA.S)
Xylitol
water
GLYCERIN
sorbitol
LEVOMENTHOL
SODIUM LAURYL SULFATE
METHYLPARABEN
CARBOXYMETHYLCELLULOSE SODIUM
POLYETHYLENE GLYCOL 4000
SODIUM CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76058-101-01 220 in 1 TUBE
2 NDC:76058-101-02 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2011-03-01


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Be sure to consult your doctor before taking any medication!
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