FDA.reportPublic FDA data

Baird Good Night

Manufacturer
JK INSPIR Co., Ltd | Kumho Dental Pharmaceutical Co., Ltd
Effective date
2021-03-17
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 23:39:03

Label at a glance#

ProductBaird Good Night
Active ingredientSODIUM FLUORIDE, SODIUM MONOFLUOROPHOSPHATE
Label structure9 sections

Indications and uses

Helps protect against cavities

Dosage and administration

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

Label contents#

Full prescribing information#

active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Monofluorophosphate (0.74%)

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

Helps protect against cavities

Uses

INDICATIONS & USAGE SECTION

Helps protect against cavities

Warnings

WARNINGS SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

OTHER SAFETY INFORMATION

Store at room temperature

Baird Good Night Toothpaste

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Baird Good Night ToothpasteBaird Good Night Toothpaste

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1737795sodium monofluorophosphate 0.74 % ToothpastePSN7
1737795sodium monofluorophosphate 0.0074 MG/MG ToothpasteSCD7
1737795sodium monofluorophosphate 0.74 % ToothpasteSY7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81239-100-022022-07-29C16284748780-1e4f33bdf-a598-d8a0-e053-dadaa90a6e4eBaird Good Night Toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81239-100-01Baird Good Night100 g in 1 TUBEPASTE, DENTIFRICE1007
81239-100-02Baird Good Night1 in 1 CARTONPASTE, DENTIFRICE17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81239-100BAIRD GOOD NIGHT (SODIUM FLUORIDE, SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [JK INSPIR CO., LTD]7Legacy NDC, 2 package rows20210319_b5992295-4a53-3930-e053-2a95a90af8e3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81239-10081239-100-01, 81239-100-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIB
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bdc38b9d-2e2b-495b-e053-2995a90a215ab5992295-4a53-3930-e053-2a95a90af8e32021-03-17WarningsExact identifier
spl id: bdc38b9d-2e2b-495b-e053-2995a90a215a
spl set id: b5992295-4a53-3930-e053-2a95a90af8e3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.