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|Product NDC Code||60319-4001|
Noble 1 plus
|Dosage Form||POWDER, DENTIFRICE|
|Labeler Name||Hankuk Bowonbio Co., Ltd|
Active ingredientA list of the active, medicinal ingredients in the drug product.
active ingredient: xylitol<text><contentstyleCode="xmChange"></content></text>
Dosage and administrationInformation about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
brush your teeth by putting appropriate amount of powder <text><contentstyleCode="xmChange"></content></text>
Inactive ingredientA list of inactive, non-medicinal ingredients in a drug product.
cetylpyridinium chloride, lactose monohydrate, corn starch, d-sorbitol, ubidecarenone, glycyrrhizae extract, tea chatechin, hydroxyapatite, propolis extract, menthol powder, spirulina color<text><contentstyleCode="xmChange"></content></text>
Indications and usageA statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
apply Proper Amount of the toothpaste on the tooth.<text><contentstyleCode="xmChange"></content></text>
PurposeInformation about the drug product’s indications for use.
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><contentstyleCode="xmChange"></content></text>
Spl product data elementsUsually a list of ingredients in a drug product.
Noble 1 Plus XYLITOL CETYLPYRIDINIUM CHLORIDE LACTOSE MONOHYDRATE STARCH, CORN SORBITOL UBIDECARENONE LICORICE TRIBASIC CALCIUM PHOSPHATE PROPOLIS WAX XYLITOL XYLITOL
Package label principal display panelThe content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
<text><contentstyleCode="xmChange"></content></text> package insert
Recent major changesA list of the section(s) that contain substantive changes that have been approved by FDA in the product labeling. The headings and subheadings, if appropriate, affected by the change are listed together with each section’s identifying number and the month and year on which the change was incorporated in the labeling.
Keep out of reach of childrenInformation pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
keep out of reach of the children<text><contentstyleCode="xmChange"></content></text>
WarningsInformation about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
■ For tooth only. ■ Avoid contact with eyes. ■ Do not swallow. If swallowed, get medical help. <text><contentstyleCode="xmChange"></content></text>
Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API