NDC Code(s) : 34362-0235-1
Packager : Caldwell Consumer Health LLC

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

The Natural Dentist Fluoride PASTE, DENTIFRICE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:34362-0235
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE(UNII: 8ZYQ1474W7)
(FLUORIDE ION - UNII:Q80VPU408O) 		FLUORIDE ION0.2430 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
SORBITOL(UNII: 506T60A25R)
XYLITOL(UNII: VCQ006KQ1E)
GOLDENSEAL(UNII: ZW3Z11D0JV)
ALOE VERA LEAF(UNII: ZY81Z83H0X)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
GLYCERIN(UNII: PDC6A3C0OX)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
HYDRATED SILICA(UNII: Y6O7T4G8P9)
XANTHAN GUM(UNII: TTV12P4NEE)
CITRUS PARADISI SEED(UNII: 12F08874Y7)
COCAMIDOPROPYL BETAINE(UNII: 5OCF3O11KX)
ECHINACEA ANGUSTIFOLIA LEAF(UNII: FS7G8S6PJ8)
CITRIC ACID MONOHYDRATE(UNII: 2968PHW8QP)
CALENDULA OFFICINALIS FLOWER(UNII: P0M7O4Y7YD)
Product Characteristics
Color white Score
Shape Size
Flavor ORANGE Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:34362-0235-1142 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part355 05/01/2011

PRINCIPAL DISPLAY PANEL

mm1.jpg

Tube Label