NDC 72265-100 Dr.pauhls Natural Tone Up Tooth

Hydrogen Peroxide Solution, Colloidal Silicon Dioxide, Tocopherol Acetate

NDC Product Code 72265-100

NDC CODE: 72265-100

Proprietary Name: Dr.pauhls Natural Tone Up Tooth What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Hydrogen Peroxide Solution, Colloidal Silicon Dioxide, Tocopherol Acetate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 72265 - Curescript

NDC 72265-100-02

Package Description: 1 TUBE in 1 CARTON > 85 g in 1 TUBE (72265-100-01)

NDC Product Information

Dr.pauhls Natural Tone Up Tooth with NDC 72265-100 is a a human over the counter drug product labeled by Curescript. The generic name of Dr.pauhls Natural Tone Up Tooth is hydrogen peroxide solution, colloidal silicon dioxide, tocopherol acetate. The product's dosage form is paste, dentifrice and is administered via topical form.

Labeler Name: Curescript

Dosage Form: Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Dr.pauhls Natural Tone Up Tooth Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROGEN PEROXIDE 1.81 g/85g
  • SILICON DIOXIDE 5.95 g/85g
  • .ALPHA.-TOCOPHEROL ACETATE .17 g/85g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • SORBITOL (UNII: 506T60A25R)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Curescript
Labeler Code: 72265
Marketing Category: UNAPPROVED DRUG OTHER - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 02-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Dr.pauhls Natural Tone Up Tooth Product Label Images

Dr.pauhls Natural Tone Up Tooth Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Hydrogen Peroxide Solution (35%) 2.14 %Colloidal silicon dioxide 7.0%Tocopherol Acetate 0.2%

Inactive Ingredients

D-Sorbitol Solution, Deionized Water , Glycerin ,Carboxymethylcellulose Sodium ,Sodium Cocoyl Glutamate ,Sodium Lauroyl Sarcosinate ,Grapefruit Seed Extract ,Enzymatically Modified Stevia ,Xylitol ,Xanthan Gum ,Melon champagne Flavor ,Citric Acid ,L-Menthol ,Mentha Oil ,Spearmint oil ,Polysorbate 60,Hydroxyapatite ,Eucalyptus Oil,Parsley Extract ,Salicylic Acid,Clove Oil

Purpose

WhiteningAnti plaqueprevent gingivitis

Warnings

■ Do not use for any other purposes except brushing your teeth.■ Do not swallow, and rinse your mouth adequately after use.■ Consult your physician or dentist and follow their directions if you swallow a large amount of toothpaste.■ Discontinue use and consult your physician or dentist if gum or mouth pain occurs after using this toothpaste■ Keep out of reach of children and guide them if they use this toothpaste.■ Store it away from high or low temperature and from direct sunlight.

Keep Out Of Reach Of Children

■ Keep out of reach of children and guide them if they use this toothpaste.

Uses

■ Promotes dental health and removal bad breath, makes tooth bright

Directions

■ Brush the teeth with a suitable amount.

* Please review the disclaimer below.