DR DEEP DEEP FRESH- glycerin paste, dentifrice

Dr Deep Deep Fresh by

Drug Labeling and Warnings

Dr Deep Deep Fresh by is a Otc medication manufactured, distributed, or labeled by MineralHouse Corporation, Sangleaf Pharm., Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Silicon Dioxide 4%, Glycerin 6.4%

INDICATIONS & USAGE

Squeeze appropriate amount of toothpaste onto your toothbrush and gently brush your teeth with a short, vertical or circular motion

DOSAGE & ADMINISTRATION

For brushing teeth

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warnings:

- For external use only

- Do not use on wounds or damaged skin

WHEN USING

When using this product, do not use other than directed

STOP USE

Stop use if allergic reaction or irritation occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

- If swallowed, get medical help or contact a Poison Control Center immediately

STORAGE AND HANDLING

Storage: Keep in a dry and cool place

INACTIVE INGREDIENT

Inactive Ingredients: Aluminum Chlorohydroxy Allantoinate, Aminocaproic Acid, D-Sorbitol Solution, Polyethylene Glycol 4000, stevgiol Glycoside, Xylitol, Citrus Paradisi (Grapefruit) Seed Extract, Camellia Sinensis Leaf Extract, Sodium Carboxymethyl Cellulose, Cacamidopropyl Betaine, L-Menthol, Mentha Piperita (Peppermint) Oil, Aqua

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR DEEP DEEP FRESH 
glycerin paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76015-110
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	7.68 g  in 120 g

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)	4.8 g  in 120 g
ALCLOXA (UNII: 18B8O9DQA2)
AMINOCAPROIC ACID (UNII: U6F3787206)
SORBITOL (UNII: 506T60A25R)
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
XYLITOL (UNII: VCQ006KQ1E)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LEVOMENTHOL (UNII: BZ1R15MTK7)
MENTHA PIPERITA (UNII: 79M2M2UDA9)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76015-110-01	1 in 1 PACKAGE	08/12/2016
1		120 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
OTC monograph final	part347	08/12/2016

Labeler - MineralHouse Corporation (557802539)

Registrant - MineralHouse Corporation (557802539)

Establishment
Name	Address	ID/FEI	Business Operations
MineralHouse Corporation		557802539	relabel(76015-110) , repack(76015-110)

Establishment
Name	Address	ID/FEI	Business Operations
Sangleaf Pharm., Co. Ltd.		689847343	manufacture(76015-110)