Sensodyne True White
Potassium Nitrate And Sodium Fluoride
Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Human Otc Drug
NDC 0135-0579Sensodyne True White also known as Potassium Nitrate And Sodium Fluoride is a human otc drug labeled by 'Glaxosmithkline Consumer Healthcare Holdings (us) Llc'. National Drug Code (NDC) number for Sensodyne True White is 0135-0579. This drug is available in dosage form of Paste. The names of the active, medicinal ingredients in Sensodyne True White drug includes Potassium Nitrate - 50 mg/g Sodium Fluoride - 1.15 mg/g . The currest status of Sensodyne True White drug is Active.
Drug Information:
| Drug NDC: | 0135-0579 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Sensodyne True White |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Sensodyne |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | True white |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Potassium Nitrate And Sodium Fluoride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Glaxosmithkline Consumer Healthcare Holdings (us) Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Paste |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | POTASSIUM NITRATE - 50 mg/g
SODIUM FLUORIDE - 1.15 mg/g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | DENTAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 21 Dec, 2015 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 23 Dec, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part356 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1038841
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | RU45X2JN0Z
8ZYQ1474W7
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 0135-0579-01 | 1 TUBE in 1 CARTON (0135-0579-01) / 85 g in 1 TUBE | 21 Dec, 2015 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose antihypersensitivity anticavity
Product Elements:
Sensodyne true white potassium nitrate and sodium fluoride potassium nitrate nitrate ion sodium fluoride fluoride ion sorbitol water glycerin hydrated silica sodium tripolyphosphate anhydrous polyethylene glycol 400 titanium dioxide sodium methyl cocoyl taurate cocamidopropyl betaine xanthan gum sodium hydroxide saccharin sodium sensodyne true white potassium nitrate and sodium fluoride potassium nitrate nitrate ion sodium fluoride fluoride ion sorbitol water glycerin hydrated silica sodium tripolyphosphate anhydrous polyethylene glycol 400 titanium dioxide sodium methyl cocoyl taurate cocamidopropyl betaine xanthan gum sodium hydroxide saccharin sodium extra fresh
Indications and Usage:
Uses ⢠builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact. ⢠aids in the prevention of dental cavities.
Warnings:
Warnings when using this product, if irritation occurs discontinue use. stop use and ask a dentist if ⢠the problem persists or worsens. sensitive teeth may indicate a serious problem that may need prompt care by a dentist. ⢠pain/sensitivity still persists after 4 weeks of use. keep out of reach of children. if more than used for brushing is accidentally swallowed, get medical help or contact a poison control center right away.
When Using:
When using this product, if irritation occurs discontinue use.
Dosage and Administration:
Directions ⢠adults and children 12 years of age and older: ⢠apply at least a 1-inch strip of the product onto a soft bristle toothbrush. ⢠brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. make sure to brush all sensitive areas of the teeth. minimize swallowing. spit out after brushing. ⢠children under 12 years: consult a dentist or doctor.
Stop Use:
Stop use and ask a dentist if ⢠the problem persists or worsens. sensitive teeth may indicate a serious problem that may need prompt care by a dentist. ⢠pain/sensitivity still persists after 4 weeks of use.
Package Label Principal Display Panel:
Principal display panel ndc 0135-0581-01 sensodyne ® true white ® toothpaste for sensitive teeth and cavity prevention mint sensitivity relief* stain prevention ⢠stain removal clinically proven ingredient for sensitivity relief* no. 1 dentist recommended brand for sensitive teeth net wt 3.0 oz (85 g) brushing with abrasive toothpaste can wear the sensitive areas of your teeth. sensodyne ® true white ® has the lowest abrasion formulation ever in a sensodyne ® toothpaste. with twice daily brushing it: ⢠is proven to relieve sensitivity pain ⢠helps to gently whiten your teeth ⢠leaves a protective shield to help prevent new stains forming ⢠freshens breath, fights cavities and helps keep gums healthy *with twice daily brushing **maximum fda sensitivity active ingredient gsk consumer healthcare warren, nj 07059 trademarks are owned by or licensed to the gsk group of companies. ©2015 gsk group of companies or its licensor. all rights reserved always follow the label 105639xa 105639xa_sensodyne true white mint_3.0 oz.jpg
Principal display panel ndc 0135-0579-01 sensodyne ® true white ® toothpaste for sensitive teeth and cavity prevention extra fresh sensitivity relief* stain prevention ⢠stain removal clinically proven ingredient for sensitivity relief* no. 1 dentist recommended brand for sensitive teeth net wt 3.0 oz (85 g) brushing with abrasive toothpaste can wear the sensitive areas of your teeth. sensodyne ® true white ® has the lowest abrasion formulation ever in a sensodyne ® toothpaste. with twice daily brushing it: ⢠is proven to relieve sensitivity pain ⢠helps to gently whiten your teeth ⢠leaves a protective shield to help prevent new stains forming ⢠freshens breath, fights cavities and helps keep gums healthy *with twice daily brushing **maximum fda sensitivity active ingredient gsk consumer healthcare warren, nj 07059 trademarks are owned by or licensed to the gsk group of companies. ©2015 gsk group of companies or its licensor. all rights reserved. always follow the label 105640xa 105640xa_sensodyne true white extra fresh_3.0 oz.jpg
Further Questions:
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