DR.PAUHLS TOOTHPAST E VANILLE BLACK TEA FLAVOR- silicon dioxide, pyridoxine hydrochloride paste, dentifrice

Dr.Pauhls TOOTHPAST E VANILLE BLACK TEA FLAVOR by

Drug Labeling and Warnings

Dr.Pauhls TOOTHPAST E VANILLE BLACK TEA FLAVOR by is a Otc medication manufactured, distributed, or labeled by CURESCRIPT, Kumho Dental Pharm. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: SILICA 13.0%, PYRIDOXINE HYDROCHLORIDE 0.05%

INACTIVE INGREDIENT

Inactive ingredients:

SORBITOL, SODIUM PCA, GLYCERIN, SODIUM LAURYL SULFATE, FLAVOR, CELLULOSE GUM, MENTHOL, XYLITOL, CITRUSGRANDIS (GRAPEFRUIT) SEED EXTRACT, SODIUM SACCHARIN HYDROXYAPATITE, CAMELLIA SINENSIS LEAF EXTRACT, CALENDULA OFFICINALIS FLOWER EXTRACT, ANTHEMIS NOBILIS FLOWER EXTRACT, PROPOLIS EXTRACT

PURPOSE

Purpose: Anti-plaque, Anti-caries, Anti-periodontitis

WARNINGS

Warnings:

Keep out of the 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 right away.

KEEP OUT OF REACH OF CHILDREN

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

Uses

Uses:

- Helps protect against cavities

- reduce plaque

- gum health

- Helps protect against gingivitis, periodontitis

- Helps freshen breath

- brightening teeth

Directions

Directions:

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.PAUHLS TOOTHPAST E VANILLE BLACK TEA FLAVOR 
silicon dioxide, pyridoxine hydrochloride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72265-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	13.0 g  in 100 g
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z)	PYRIDOXINE	0.05 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72265-030-02	1 in 1 CARTON	07/01/2018
1	NDC: 72265-030-01	100 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2018

Labeler - CURESCRIPT (694894509)

Registrant - CURESCRIPT (694894509)

Establishment
Name	Address	ID/FEI	Business Operations
Kumho Dental Pharm. Co., Ltd.		631133766	manufacture(72265-030)