TITAD FRESH BREATH PLUS TOOTH by KMPHARMACEUTICAL CO.,LTD / KMPHARMACEUTICAL Co.,Ltd.

TITAD FRESH BREATH PLUS TOOTH by

Drug Labeling and Warnings

TITAD FRESH BREATH PLUS TOOTH by is a Otc medication manufactured, distributed, or labeled by KMPHARMACEUTICAL CO.,LTD, KMPHARMACEUTICAL Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TITAD FRESH BREATH PLUS TOOTH- sodium monofluorophosphate paste, dentifrice 
KMPHARMACEUTICAL CO.,LTD

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Active ingredient(s)

Sodium monofluorophosphate 0.76% (0.15% w/v fluoride ion)

Inactive ingredients

Sorbitol, Water, Silica, Hydrated Silica, Glycerin, Flavor, Sodium PCA, Cellulose Gum, Sodium Cocoyl Glutamate, Xylitol, Tetrasodium pyrophosphate, Lauramidopropyl Betaine, Stevia Rebaudiana Extract, Sodium Bicarbonate, Scutellaria Baicalensis Root Extract, Salvia Officinalis (Sage) Extract, Camellia Sinensis Leaf Extract, Tocopheryl Acetate, Menthol, Myrrh Tinc, Chamomile tincture, Rhatany tincture, Chamomilla Recutita (Matricaria) Extract

Fragrance allergen : D-Limonene, Eugenol, Isoeugenol, Linalool

Purpose

Anticavity

Warnings

■ Keep out of the reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Keep out of the reach of children

Use(s)

aid in the prevention of dental cavities

Directions

■ adults and children 2 years of age and older : brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician

■ children 2 to 6 years : use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)

■ children under 2 years : ask a dentist or physician

Other Information

■ Alright container, Store in normal temperature (1~30℃)

Questions

overseas@dailynco.com

www.titad.kr

TITAD FRESH BREATH PLUS TOOTHPASTE 100g

TITAD FRESH BREATH PLUS TOOTHPASTE 20g

TITAD FRESH BREATH PLUS TOOTH 
sodium monofluorophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50555-200
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.76 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
TETRASODIUM PYROPHOSPHATE (UNII: O352864B8Z)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
CELLULOSE GUM (UNII: K679OBS311)
STEVIA REBAUDIANA WHOLE (UNII: 6U422Y08O2)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
WATER (UNII: 059QF0KO0R)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
SAGE (UNII: 065C5D077J)
ISOEUGENOL (UNII: 5M0MWY797U)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
EUGENOL (UNII: 3T8H1794QW)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM PCA (UNII: 469OTG57A2)
LINALOOL (UNII: D81QY6I88E)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50555-200-02	1 in 1 CARTON	10/01/2024	12/31/2025
1	NDC: 50555-200-01	100 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 50555-200-04	1 in 1 CARTON	10/01/2024	12/31/2025
2	NDC: 50555-200-03	20 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 Drug	M021	10/01/2024	12/31/2025

Labeler - KMPHARMACEUTICAL CO.,LTD (689850153)

Establishment
Name	Address	ID/FEI	Business Operations
KMPHARMACEUTICAL Co.,Ltd.		689850153	manufacture(50555-200)

Revised: 3/2026

Document Id: 4c30d671-f40f-38ff-e063-6394a90a1970

34390-5

Set id: 263439da-ffdb-3c6a-e063-6394a90abbf1

Version: 4

Effective Time: 20260304