NDC 42507-552 Hyvee Complete Care Fresh Mint

NDC Product Code 42507-552

NDC 42507-552-33

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hyvee Complete Care Fresh Mint with NDC 42507-552 is a product labeled by Hyvee Inc.. The generic name of Hyvee Complete Care Fresh Mint is . The product's dosage form is and is administered via form.

Labeler Name: Hyvee Inc.

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)
  • SORBITOL (UNII: 506T60A25R)
  • ALCOHOL (UNII: 3K9958V90M)
  • POLOXAMER 407 (UNII: TUF2IVW3M2)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • EUCALYPTOL (UNII: RV6J6604TK)
  • METHYL SALICYLATE (UNII: LAV5U5022Y)
  • THYMOL (UNII: 3J50XA376E)
  • PHOSPHORIC ACID (UNII: E4GA8884NN)
  • SUCRALOSE (UNII: 96K6UQ3ZD4)
  • MENTHOL (UNII: L7T10EIP3A)
  • SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Hyvee Inc.
Labeler Code: 42507
Start Marketing Date: 09-12-2013 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Information for Patients

Fluoride

Fluoride is pronounced as (floor' ide)

Why is fluoride medication prescribed?
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 usu...
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Hyvee Complete Care Fresh Mint Product Label Images

Hyvee Complete Care Fresh Mint 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 Ingredient

Sodium Fluoride 0.02% (0.01% w/v Fluoride ion)

Purpose

Antigingivitis/Antiplaque

Uses

  • To help reduce and preventplaquegingivitis

Warnings

Do not use in children under 12 years of age

Keep Out Of Reach Of Children

If more than used for rinsing is accidentally ingested, get medical help or contact a Poison Control Center immediately

Directions

  • Rinse full strength for 30 seconds with 20 mL (2/3 fluid ounce or 4 teaspoonfuls) morning and nightDo not swallow

Other Information

  • Store at room temperatureCold weather may cloud this product. Its antiseptic properties are not affected.

Inactive Ingredients

Water (Aqua), Sorbitol, Alcohol (21.6%), Poloxamer 407, Sodium Lauryl Sulfate, Eucalyptol, Flavor, Methyl Salicylate, Thymol, Phosphoric Acid, Sucralose, Menthol, Disodium Phosphate, Red 40 (CI 16035), Blue 1 (CI 42090).

* Please review the disclaimer below.