HOUSE LIVING- sodium fluoride,potassium nitrate paste

House Living by

Drug Labeling and Warnings

House Living by is a Otc medication manufactured, distributed, or labeled by Guangzhou Beauty Cosmetic Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

SODIUM FLUORIDE 0.15%

Potassium Nitrate 5%

Purpose

Antihypersensitivity

Anticavity

Use

bulids increasing protection against painful sensitivity of the teeth due to cold,heat,acids,sweets or contact

aids in the privention of dental cavities

Warning

Stop use and ask a dentist if

the problem pensists os worsens,sensitive teeth may indicate a serious problem that may prompt care by a dentist

pain/sensitivity still persists after 4 weeks of use.

Directions

Adults and children 2 years of age and older:brush teeth thoroughly, preferably after meals or at least twice a day or use as directed by a dentist or doctor.

instruct children 6 years of age in good brushing and rinsing habits(to minimize swallowing)

suprevise children as necessary untill capable of using without supervision.

children under 2 years of age :consult a dentist or doctor

Inactive Ingredients

Water,Silica (Thickening 10 & Friction 4)
,Sodium Lauryl Alcohol,Sorbitol,Polyethylene Glycol 300,Sodium Carboxymethylcellulose,Flavor,Sodium Saccharin,Titanium Dioxide,Sodium Pyrophosphate,PEG/PPG 116/66 copolymer
Sodium Hydroxide,Acid Yellow 23,Acid Blue 1

KEEP OUT OF REACH OF CHILDREN

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



If more than used for brushing is accidently swallowed get medical help or contact a poison control center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUSE LIVING 
sodium fluoride,potassium nitrate paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71704-002
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	5 g  in 100 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.15 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEG/PPG-116/66 COPOLYMER (UNII: JP0CK963E0)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SODIUM PYROPHOSPHATE DECAHYDRATE (UNII: IY3DKB96QW)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71704-002-01	24 in 1 CARTON	07/10/2016
1		113 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 not final	part356	07/10/2016

Labeler - Guangzhou Beauty Cosmetic Co., Ltd (528735414)

Registrant - Guangzhou Beauty Cosmetic Co., Ltd (528735414)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Beauty Cosmetic Co., Ltd		528735414	manufacture(71704-002)