NDC 0135-1250 Natean Clean Plus Sensitivity Relief

Potassium Nitrate, Sodium Fluoride

NDC Product Code 0135-1250

NDC CODE: 0135-1250

Proprietary Name: Natean Clean Plus Sensitivity Relief 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: Potassium Nitrate, Sodium Fluoride 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.

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404 - SOOTHING MINT)

NDC Code Structure

  • 0135 - Glaxosmithkline Consumer Healthcare Holdings (us) Llc

NDC 0135-1250-01

Package Description: 1 TUBE in 1 CARTON > 133 g in 1 TUBE

NDC Product Information

Natean Clean Plus Sensitivity Relief with NDC 0135-1250 is a a human over the counter drug product labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The generic name of Natean Clean Plus Sensitivity Relief is potassium nitrate, sodium fluoride. The product's dosage form is paste and is administered via oral form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1086243.

Dosage Form: Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Natean Clean Plus Sensitivity Relief 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.


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.

  • WATER (UNII: 059QF0KO0R)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • SORBITOL (UNII: 506T60A25R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • REBAUDIOSIDE A (UNII: B3FUD0528F)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)

Administration Route(s)

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

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Labeler Code: 0135
FDA Application Number: part356 What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 01-03-2022 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Natean Clean Plus Sensitivity Relief Product Label Images

Natean Clean Plus Sensitivity Relief 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

Potassium nitrate 5%Sodium fluoride 0.25% (0.15% w/v fluoride ion)

Purposes

AntihypersensitivityAnticavity

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

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.

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.

Other Information

  • •do not store above 25°C (77F°)

Inactive Ingredients

Water, hydrated silica, sorbitol, glycerin, flavor, cocamidopropyl betaine, sodium cocoyl glutamate, xanthan gum, rebaudioside A, cocos nucifera (coconut) oil, aloe barbadensis leaf extract, maltodextrin

Additional Information

  • ALWAYS FOLLOW THE LABELNatean was created by a small passionate team of scientists and herbalists on a mission to give you the best of what nature and science can offer, while minimizing our impact to the planet. Our toothpastes expertly balance powerful, scientifically studied ingredients with botanicals for a clean you can feel, and a clean you can feel good about.NATEAN-INSPIRED BY NATURE AND DESIGNED TO BE CLEANRELIEVES SENSITIVE TEETH AND LEAVES YOUR MOUTH FEELING CLEAN AND FRESH •Infused with natural orange blossom and mint flavor, and extracts from aloe vera and coconut •Contains fluoride to fight cavities •Helps control tartar build-up with twice daily brushing*No animal origin materials used in the processing of these products. Contains no animal ingredients or derivatives.†Recycling facilities for this product may not exist in your areaBPA-FREE TUBETube contains post consumer recycled plasticRecycleable carton, tube & capDistributed by: Alacer Corp. Carlisle, PA 17013© 2021 Alacer Corp.www.nateantoothpaste.com

* Please review the disclaimer below.