NEW DOCTOR AG PLUS GOLD- sodium monofluorophosphate paste, dentifrice

NEW DOCTOR AG PLUS by

Drug Labeling and Warnings

NEW DOCTOR AG PLUS by is a Otc medication manufactured, distributed, or labeled by HANIL PHARMACEUTICAL CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT: Sodium Monofluorophosphate

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:

D-Sorbitol, Glycerin, Sodium  Saccharin, Chitosan, Xylitol, Sodium Lauryl Sulfate, Menthol, Peppermint, Sodium Benzoate, Green tea extract, Sodium Carboxyl Cellulose,
Siver, Water, Triclosan, Siliccon Dioxide

PURPOSE

PURPOSE: ANTICAVITY

WARNINGS

WARNINGS:
WHEN USING THIS PRODUCT DO NOT USE FOR SENSITIVITY LONGER THAN FOUR WEEKS UNLESS RECOMMENDED BY A DENTIST.
STOP USE AND ASK A DENTIST IF THE SENSITIVITY PROBLEM PERSISTS OR WORSENS.
SENSITIVE TEETH MAY NEED PROMPT CARE.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN:

IF ACCIDENTALLY SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INDICATIONS & USAGE

INDICATION AND USAGE:

ADULTS AT LEAST A HALF-INCH STRIP OF THE PRODUCT ONTO A SOFT BRISTLED TOOTH BRUSH.
BRUSH TEETH THOROUGHLY FOR AT LEAST 3 MINUTES TWICE A DAY (MORNING AND EVENING)
UNDER 12 YRS: ASK A DENTIST

DOSAGE & ADMINISTRATION

DOSAGE AND ADMINISTRATION:

ADULTS AT LEAST A HALF-INCH STRIP OF THE PRODUCT ONTO A SOFT BRISTLED TOOTH BRUSH.
BRUSH TEETH THOROUGHLY FOR AT LEAST 3 MINUTES TWICE A DAY (MORNING AND EVENING)
UNDER 12 YRS: ASK A DENTIST

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEW DOCTOR AG PLUS  GOLD
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75984-001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM MONOFLUOROPHOSPHATE	0.15 g  in 150 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
XYLITOL (UNII: VCQ006KQ1E)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
MENTHOL (UNII: L7T10EIP3A)
PEPPERMINT (UNII: V95R5KMY2B)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SILVER (UNII: 3M4G523W1G)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75984-001-01	150 g in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	09/01/2010

Labeler - HANIL PHARMACEUTICAL CO., LTD. (688197087)

Registrant - HANIL PHARMACEUTICAL CO., LTD. (688197087)

Establishment
Name	Address	ID/FEI	Business Operations
HANIL PHARMACEUTICAL CO., LTD.		688197087	manufacture