TEETH WHITENING POWDER powder

Teeth Whitening Powder by

Drug Labeling and Warnings

Teeth Whitening Powder by is a Otc medication manufactured, distributed, or labeled by Shenzhen Hengkaifeng Commerce and Trade Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Charcoal Powder 10.94%

Purpose

Teeth Whitening

Use

Enhance your teeth cleaning routine with the teeth whitening powder .
The powerful formula works to care for teeth and gums, remove
plaque and tartar, gently lift stains and freshen breath for an overall
deep clean.

Warnings

WARNING: to avoid danger of suffocation. keep this plastic bag
away from babiés and children.do not use this bag incribs, beds,
carriages or play pens.this bag is not a toy.

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

Directions Of Safe Use:

Easy to use anytime, anywhere, simply squeeze an appropriate amount
of teeth powder dips your toothbrush, gently brush your teeth for 2
minutes, and then rinse your mouth thoroughly with water. Take it
with you anywhere, anytime, so you can easily enjoy the benefits of
whitening!

Inactive ingredients

Aqua, Sorbitol, Hydrated Silica, Disodium Pyrophosphate, Monosodium
Citrate, Sodium Lauryl Sulfate, Aroma, Alumina, Cellulose Gum,
Cyclodextrin, Mannitol, Microcrystalline Cellulose,
Sodium Saccharin, Phthalimidoperoxycaproic Acid, Hydrogenated
Lecithin, Hydroxypropyl Starch Phosphate, Zea Mays Starch,
Tetrapotassium Pyrophosphate, Hydroxyapatite, Eugenol, Citric Acid.

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TEETH WHITENING POWDER 
teeth whitening powder powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84117-010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	10.94 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
MONOSODIUM CITRATE (UNII: 68538UP9SE)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALUMINUM OXIDE (UNII: LMI26O6933)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
CYCLODEXTRINS (UNII: 7E6SK9QDT8)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
PHTHALIMIDOPEROXYCAPROIC ACID (UNII: 5OEJ6FAL6C)
POTASSIUM PYROPHOSPHATE (UNII: B9W4019H5G)
EUGENOL (UNII: 3T8H1794QW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84117-010-01	50 g in 1 CANISTER; Type 0: Not a Combination Product	05/27/2024
2	NDC: 84117-010-02	30 g in 1 CANISTER; Type 0: Not a Combination Product	05/27/2024
3	NDC: 84117-010-03	60 g in 1 CANISTER; Type 0: Not a Combination Product	05/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	05/27/2024

Labeler - Shenzhen Hengkaifeng Commerce and Trade Co., Ltd (444722774)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Hengkaifeng Commerce and Trade Co., Ltd		444722774	manufacture(84117-010) , label(84117-010)