NDC 37000-856 Crest Pro-health Hd
Stannous Fluoride Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37000 - The Procter & Gamble Manufacturing Company
- 37000-856 - Crest Pro-health Hd
Product Characteristics
Product Packages
NDC Code 37000-856-04
Package Description: 1 KIT in 1 CARTON * 113 g in 1 TUBE * 65 g in 1 TUBE
Product Details
What is NDC 37000-856?
What are the uses for Crest Pro-health Hd?
Which are Crest Pro-health Hd UNII Codes?
The UNII codes for the active ingredients in this product are:
- STANNOUS FLUORIDE (UNII: 3FTR44B32Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Crest Pro-health Hd Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- WATER (UNII: 059QF0KO0R)
- ZINC LACTATE (UNII: 2GXR25858Y)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Crest Pro-health Hd?
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.00454 MG/MG Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.15 % ) Toothpaste
* Please review the disclaimer below.
Patient Education
Fluoride
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[1] 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.
[3] 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.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] 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.
[8] 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.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".