NDC 58933-020 Crest Complete Multi-benefit Whitening Plus Scope

NDC Product Code 58933-020

NDC CODE: 58933-020

Proprietary Name: Crest Complete Multi-benefit Whitening Plus Scope What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: 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.

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
PEPPERMINT (C73408)

NDC Code Structure

NDC 58933-020-03

Package Description: 1 TUBE in 1 CARTON > 76.5 g in 1 TUBE

NDC 58933-020-06

Package Description: 1 TUBE in 1 CARTON > 175 g in 1 TUBE

NDC 58933-020-08

Package Description: 1 TUBE in 1 CARTON > 226 g in 1 TUBE

NDC 58933-020-85

Package Description: 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

Crest Complete Multi-benefit Whitening Plus Scope with NDC 58933-020 is a product labeled by Procter & Gamble Manufactura, S. De R.l. De C.v.. The generic name of Crest Complete Multi-benefit Whitening Plus Scope is . The product's dosage form is and is administered via form.

Labeler Name: Procter & Gamble Manufactura, S. De R.l. De C.v.

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.

  • SORBITOL (UNII: 506T60A25R)
  • WATER (UNII: 059QF0KO0R)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • ALCOHOL (UNII: 3K9958V90M)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • SACCHARIN SODIUM (UNII: SB8ZUX40TY)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Labeler Information

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

Labeler Name: Procter & Gamble Manufactura, S. De R.l. De C.v.
Labeler Code: 58933
Start Marketing Date: 07-01-2011 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: 12-31-2020 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.

Crest Complete Multi-benefit Whitening Plus Scope Product Label Images

Crest Complete Multi-benefit Whitening Plus Scope 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 0.243%

(0.15% w/v fluoride ion)

Purpose

Anticavity toothpaste

Otc - Keep Out Of Reach Of Children

Keep out of reach of children under 6 yrs. 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 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentistdo not swallowto minimize swallowing use a pea-sized amount in children under 6supervise children’s brushing until good habits are establishedchildren under 2 yrs.: ask a dentist

Inactive Ingredients

Sorbitol, water, hydrated silica, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, alcohol (0.7%), xanthan gum, sodium saccharin, glycerin, carbomer, cellulose gum, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, titanium dioxide, blue 1, yellow 5

Questions?

1-800-492-7378

Other

DISTR. BY/POR PROCTER & GAMBLE,

CINCINNATI, OH 45202

* Please review the disclaimer below.