OraBrite description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

OraBrite

Oraline, Inc.
Oraline, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

DRUG FACTS

ACTIVE INGREDIENT:

Sodium Fluoride 0.22%

(Total Fluoride Content - 1000 ppm approx.)

Purpose

PURPOSE: Anticavity Toothpaste.

Keep Out Of Reach Of Children

WARNINGS: Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Use

USE: Helps protect against cavities.

Warnings

WARNINGS: Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DIRECTIONS:

Adults and children 2 tears of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Instruct children under 6 years of age in god brushing and rinsing habits. (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 2 years of age: Consult a dentist or doctor.

Inactive Ingredients

INACTIVE INGREDIENTS:

Hydrated Silica, Sorbitol, Deionized Water, Methyl Paraben Sodium, Propyl Paraben Sodium, Sodium Lauryl Sulfate, Sodium Carboxymethylcellulose, Flavor, Sodium Saccharin.

Package Label

Distributed by Oraline Inc., 823 NYS RT 13, Cortland, N.Y. 13045

OraBrite

Mint Flavor with Fluoride

NET WT 1.50 oz.

Mfg. Date and Batch No. on crimp.

Product of China, produced for Oraline. 888-296-6730.  www.oraline.net

OraBrite


OraBrite

SODIUM FLUORIDE PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54371-471
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.22 g

Inactive Ingredients

Ingredient Name Strength
HYDRATED SILICA
sorbitol
water
METHYLPARABEN SODIUM
PROPYLPARABEN SODIUM
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54371-471-01 24 in 1 TUBE
2 NDC:54371-471-02 43 in 1 TUBE
3 NDC:54371-471-03 78 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2011-10-31


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.