NDC 72655-300 Eversmile Alignerfresh Enamel Guard
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72655 - Everbrands, Inc.
- 72655-300 - Eversmile Alignerfresh Enamel Guard
Product Characteristics
Product Packages
NDC Code 72655-300-01
Package Description: 1 BOTTLE, PUMP in 1 PACKAGE / 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 72655-300?
What are the uses for Eversmile Alignerfresh Enamel Guard?
Which are Eversmile Alignerfresh Enamel Guard 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 Eversmile Alignerfresh Enamel Guard 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:
- ETIDRONIC ACID (UNII: M2F465ROXU)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- POVIDONE K30 (UNII: U725QWY32X)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Eversmile Alignerfresh Enamel Guard?
- RxCUI: 2597250 - sodium fluoride 0.05 % Oral Foam
- RxCUI: 2597250 - sodium fluoride 0.5 MG/ML Oral Foam
- RxCUI: 2597250 - sodium fluoride 0.05 % (fluoride ion 0.0225 % ) Oral Foam
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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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[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".