NDC 70108-015 Thomas And Friends
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70108 - Ashtel Studios, Inc.
- 70108-015 - Thomas And Friends
Product Packages
NDC Code 70108-015-01
Package Description: 100 mL in 1 TUBE
Product Details
What is NDC 70108-015?
What are the uses for Thomas And Friends?
Which are Thomas And Friends UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Thomas And Friends 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:
- SORBITOL (UNII: 506T60A25R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Thomas And Friends?
- RxCUI: 416783 - sodium fluoride 0.24 % Toothpaste
- RxCUI: 416783 - sodium fluoride 0.0024 MG/MG Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (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.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".