NDC 64893-220 Dr. Fresh Dailies Travel

NDC Product Code 64893-220

NDC 64893-220-00

Package Description: 1 TUBE in 1 KIT > 24 g in 1 TUBE

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

NDC Product Information

Dr. Fresh Dailies Travel with NDC 64893-220 is a product labeled by Dr. Fresh, Inc.. The generic name of Dr. Fresh Dailies Travel is . The product's dosage form is and is administered via form.

Labeler Name: Dr. Fresh, Inc.

Dosage Form: -

Product Type: 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.

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.

  • DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
  • METHYL SALICYLATE (UNII: LAV5U5022Y)
  • SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
  • SACCHARIN SODIUM (UNII: SB8ZUX40TY)

Product Labeler Information

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

Labeler Name: Dr. Fresh, Inc.
Labeler Code: 64893
Start Marketing Date: 07-16-2010 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Dr. Fresh Dailies Travel Product Label Images

Dr. Fresh Dailies Travel 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 Monofluorophosphate 0.76 percent (0.15 percent w v fluoride ion)

Purpose

Anticavity

Use

Helps protect against cavities

Keep Out Of Reach Of Children Under 6 Years Of Age.

If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.Children under the age of 6:   Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)Children under 2 years of age: Ask a dentist or doctor.

Inactive Ingredients

Dicalcium phosphate dihydrate, water, glycerin, sodium lauryl sulfate, cellulose gum, flavor, tetrasodium pyrophosphate, sodium saccharin

Otc - Questions

Questions or CommentsToll Free: 1-866-DR-Fresh (1-866-373-7374) or comments drfresh.comVisit  us online at: www.drfresh.com


Monday-Friday 8:30 am  to 5:30 pm

* Please review the disclaimer below.