Label: NOBLE S PLUS- silver paste, dentifrice

  • NDC Code(s): 60319-2001-1
  • Packager: Hankuk Bowonbio Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 3, 2019

If you are a consumer or patient please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    active ingredient: silver<text><content
    styleCode="xmChange">
    </content></text>

  • INACTIVE INGREDIENT

    inactive ingredient: tocopherol acetate, sodium monofluorophosphate, D-sorbitol, carboxymethylcellulose sodium, sodium lauryl sulfate, sodium saccharin, green tea, xylitol, grapefruit seed, aloe vera, polyethylene glycol 1500, triclosan, stearic acid, polysorbate 80, apple juice, water, L-menthol, silicon dioxide<text><content
    styleCode="xmChange">
    </content></text>

  • PURPOSE

    whiten and strong teeth

    removal of bad breath

    prevention of gingivitis and periodontitis

    prevention of periodontal diseases and gum diseases

    removal of dental plaque<text><content
    styleCode="xmChange">
    </content></text>



  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children<text><content
    styleCode="xmChange">
    </content></text>

  • INDICATIONS & USAGE

    apply Proper Amount of the toothpaste on the tooth.

  • WARNINGS

    ■ For tooth only.

    ■ Avoid contact with eyes.

    ■ Do not swallow. If swallowed, get medical help.<text><content
    styleCode="xmChange">
    </content></text>



  • DOSAGE & ADMINISTRATION

    brush your teeth by putting appropriate amount of tooth paste<text><content
    styleCode="xmChange">
    </content></text>

  • PRINCIPAL DISPLAY PANEL

    package insert
  • INGREDIENTS AND APPEARANCE
    NOBLE S PLUS 
    silver paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60319-2001
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER0.7 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)  
    SORBITOL (UNII: 506T60A25R)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    XYLITOL (UNII: VCQ006KQ1E)  
    GRAPEFRUIT SEED OIL (UNII: 598D944HOL)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    APPLE JUICE (UNII: 9871T0PD5P)  
    LEVOMENTHOL (UNII: BZ1R15MTK7)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60319-2001-1130 g in 1 TUBE; Type 0: Not a Combination Product12/01/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/19/2011
    Labeler - Hankuk Bowonbio Co., Ltd (690045133)
    Registrant - Hankuk Bowonbio Co., Ltd (690045133)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hankuk Bowonbio Co., Ltd690045133manufacture(60319-2001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!