BAIRD GOOD NIGHT- sodium fluoride, sodium monofluorophosphate paste, dentifrice 
JK INSPIR Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Baird Good Night Toothpaste

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

Baird Good Night Toothpaste

BAIRD GOOD NIGHT 
sodium fluoride, sodium monofluorophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81239-100
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.74 g  in 100 g
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.0976 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81239-100-021 in 1 CARTON12/03/2020
1NDC:81239-100-01100 g in 1 TUBE; Type 0: Not a Combination Product
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35512/03/2020
Labeler - JK INSPIR Co., Ltd (694700174)
Registrant - JK INSPIR Co., Ltd (694700174)
Establishment
NameAddressID/FEIBusiness Operations
Kumho Dental Pharmaceutical Co., Ltd631133766manufacture(81239-100)

Revised: 3/2021
Document Id: bdc38b9d-2e2b-495b-e053-2995a90a215a
Set id: b5992295-4a53-3930-e053-2a95a90af8e3
Version: 7
Effective Time: 20210317
 
JK INSPIR Co., Ltd