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  4. NDC Product Code: 35000-952 Colgate Optic White Platinum Anticavity Fluoride

NDC 35000-952 Colgate Optic White Platinum Anticavity Fluoride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 35000-952?
  5. Colgate Optic White Platinum Anticavity Fluoride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
35000-952
Proprietary Name:
Colgate Optic White Platinum Anticavity Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Colgate-palmolive Company
Labeler Code:
35000
Product Label ID:
a71d468a-5535-4f3b-acd5-d580f3a21404
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404)

Product Packages

NDC Code 35000-952-86

Package Description: 1 TUBE in 1 CARTON / 127 g in 1 TUBE

NDC Code 35000-952-93

Package Description: 1 TUBE in 1 CARTON / 96 g in 1 TUBE

Product Details

What is NDC 35000-952?

The NDC code 35000-952 is assigned by the FDA to the product Colgate Optic White Platinum Anticavity Fluoride which is product labeled by Colgate-palmolive Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 35000-952-86 1 tube in 1 carton / 127 g in 1 tube, 35000-952-93 1 tube in 1 carton / 96 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Colgate Optic White Platinum Anticavity Fluoride?

Adults and children 2 years of age and olderbrush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physicianchildren 2 to 6 yearsuse only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)children under 2 yearsask a dentist or physician

Which are Colgate Optic White Platinum Anticavity Fluoride UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Colgate Optic White Platinum Anticavity Fluoride 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:

What is the NDC to RxNorm Crosswalk for Colgate Optic White Platinum Anticavity Fluoride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste

* Please review the disclaimer below.

Product Footnotes

[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".