BAIRD GOOD NIGHT- sodium fluoride, sodium monofluorophosphate paste, dentifrice

Baird Good Night by

Drug Labeling and Warnings

Baird Good Night by is a Otc medication manufactured, distributed, or labeled by JK INSPIR Co., Ltd, Kumho Dental Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

active ingredient

Sodium Monofluorophosphate (0.74%)

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

If more than what is used for brushing is swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right

away.

Purpose

Helps protect against cavities

Uses

Helps protect against cavities

Warnings

Stop use and ask a doctor if you experience any problems in your gums, mouth, or teeth.

Directions

Adults and children 2 years of age and older

Brush tooth thoroughly, preferably after each meal, or at least

twice a day, or as directed by your dentist. Do not swallow.

Children 2 to 6 years

To minimize swallowing, use a pea-sized amount and

supervising brushing until good habits are established.

Children under 2 years

Ask a dentist or physician

Inactive Ingredients

Sorbitol, water, hydrated silica, sodium pca, glycerin, sodium methylcocoytaurate,

tetrasodium pyrophosphate, cellulose gum, flavor, scutellaria baicalensis root extract,

propolis extract, mentha piperita (peppermint) oil, tocopherylacetate, glucosylstevioside,

xylitol, menthol, pyridoxine hcl, anthemis nobilis flower extract, camellia sinensis leaf extract,

Rosmarinus officinalis (rosemary) leaf extract, salvia officinalis (sage) leaf extract, ascorbic

acid, ecklonia cava extract, commiphora myrrha resin extract, krameria triandra root extract,

chamomilla recutita (matricaria) flower extract

Other Information

Store at room temperature

Baird Good Night Toothpaste

INGREDIENTS AND APPEARANCE

BAIRD GOOD NIGHT 
sodium fluoride, sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81239-100
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.74 g  in 100 g
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.0976 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81239-100-02	1 in 1 CARTON	12/03/2020
1	NDC: 81239-100-01	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
OTC monograph final	part355	12/03/2020

Labeler - JK INSPIR Co., Ltd (694700174)

Registrant - JK INSPIR Co., Ltd (694700174)

Establishment
Name	Address	ID/FEI	Business Operations
Kumho Dental Pharmaceutical Co., Ltd		631133766	manufacture(81239-100)