Sensodyne Sensitivity And Gum Whitening
Stannous Fluoride
Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Human Otc Drug
NDC 0135-5024Sensodyne Sensitivity And Gum Whitening also known as Stannous Fluoride is a human otc drug labeled by 'Glaxosmithkline Consumer Healthcare Holdings (us) Llc'. National Drug Code (NDC) number for Sensodyne Sensitivity And Gum Whitening is 0135-5024. This drug is available in dosage form of Paste. The names of the active, medicinal ingredients in Sensodyne Sensitivity And Gum Whitening drug includes Stannous Fluoride - 1.1 mg/g . The currest status of Sensodyne Sensitivity And Gum Whitening drug is Active.
Drug Information:
| Drug NDC: | 0135-5024 |
| 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 Sensitivity And Gum Whitening |
| 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: | Sensitivity and Gum Whitening |
| 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: | Stannous 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: | STANNOUS FLUORIDE - 1.1 mg/g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | ORAL
|
| 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: | 06 Jan, 2020 |
| 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: | 416784
|
| 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: | 3FTR44B32Q
|
| 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 |
|---|
| 0135-5024-01 | 1 TUBE in 1 CARTON (0135-5024-01) / 96.4 g in 1 TUBE | 06 Jan, 2020 | N/A | No |
| 0135-5024-02 | 1 TUBE in 1 CARTON (0135-5024-02) / 65.2 g in 1 TUBE | 06 Jan, 2020 | 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:
Purposes anticavity, antigingivitis, antihypersensitivity
Product Elements:
Sensodyne sensitivity and gum mint stannous fluoride stannous fluoride fluoride ion glycerin polyethylene glycol 400 hydrated silica sodium tripolyphosphate, unspecified form sodium lauryl sulfate titanium dioxide cocamidopropyl betaine saccharin sodium sensodyne sensitivity and gum whitening stannous fluoride stannous fluoride fluoride ion glycerin polyethylene glycol 400 hydrated silica sodium tripolyphosphate, unspecified form sodium lauryl sulfate titanium dioxide cocamidopropyl betaine saccharin sodium sensodyne sensitivity and gum clean and fresh stannous fluoride stannous fluoride fluoride ion glycerin polyethylene glycol 400 hydrated silica sodium tripolyphosphate anhydrous sodium lauryl sulfate titanium dioxide cocamidopropyl betaine saccharin sodium
Indications and Usage:
Uses ⢠aids in the prevention of dental cavities. ⢠helps control bleeding gums. ⢠helps interfere with harmful effects of plaque associated with gingivitis. ⢠builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact.
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. ⢠gingivitis, bleeding, or redness persists for more than 2 weeks. ⢠you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. these maybe signs or symptoms of periodontitis, a serious form of gum disease. 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 of age: 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. ⢠gingivitis, bleeding, or redness persists for more than 2 weeks. ⢠you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. these maybe signs or symptoms of periodontitis, a serious form of gum disease.
Package Label Principal Display Panel:
Principal display panel ndc 0135-5024-01 sensodyne sensitivity & gum with fluoride toothpaste for sensitive teeth, gingivitis and cavity prevention new wt 3.4 oz (96.4 g) dual action toothpaste 9 out of 10 dentists recommended brand #1 dentist recommend brand for sensitive teeth improves gum health whitening gsk ©2019 gsk group of companies or its licensor. 62000000043416 sensodyne sensitivity & gum whitening 3.4 oz carton
Principal display panel ndc 0135-5023-01 sensodyne sensitivity & gum with fluoride toothpaste for sensitive teeth, gingivitis and cavity prevention new wt 3.4 oz (96.4 g) dual action toothpaste 9 out of 10 dentists recommended brand #1 dentist recommend brand for sensitive teeth improves gum health mint gsk ©2019 gsk group of companies or its licensor. 62000000043415 sensodyne sensitivity & gum mint 3.4 oz carton
Principal display panel ndc 0135-5025-01 sensodyne sensitivity & gum with fluoride new fresh taste toothpaste for sensitive teeth, gingivitis and cavity prevention new wt 3.4 oz (96.4 g) dual action toothpaste 9 out of 10 dentists recommended brand #1 dentist recommend brand for sensitive teeth improves gum health clean & fresh gsk ©2020 gsk group of companies or its licensor. 62000000050444 sensodyne sensitivity & gum clean & fresh 3.4 oz carton
Further Questions:
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