NBF GINGIVAL- sodium monofluorophosphate gel

NBF Gingival by

Drug Labeling and Warnings

NBF Gingival by is a Otc medication manufactured, distributed, or labeled by NanoCureTech, Sungwon Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

active ingredient: sodium monofluorophosphate

INACTIVE INGREDIENT

inactive ingredient: silicon dioxide, triclosan, glycerin, d-sorbitol, polyethylene glycol, chitosan oligosaccharide, carboxymethylcellulose sodium, propolis extract, xylitol, sacccharin sodium hydroate, peppermint oil, l-menthol, sodium benzoate, ascorbic acid, tocopherol, purified water

PURPOSE

■ prevention of gingival disease

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply toothpast on soft bristle toothbrush and brush

WARNINGS

if irritation occurs when using this product, discontinue use

DOSAGE & ADMINISTRATION

■ apply three times a day after meals

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NBF GINGIVAL 
sodium monofluorophosphate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 23636-1001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM MONOFLUOROPHOSPHATE	0.4 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TRICLOSAN (UNII: 4NM5039Y5X)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITOL (UNII: 506T60A25R)
CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
XYLITOL (UNII: VCQ006KQ1E)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
MENTHA PIPERITA (UNII: 79M2M2UDA9)
MENTHOL (UNII: L7T10EIP3A)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 23636-1001-1	30 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/11/2011

Labeler - NanoCureTech (557799555)

Registrant - NanoCureTech (557799555)

Establishment
Name	Address	ID/FEI	Business Operations
Sungwon Pharmaceutical Co., Ltd		689787898	manufacture