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Data / Drug companies / Colgate Oral Pharmaceuticals, Inc.

Colgate Oral Pharmaceuticals, Inc.: 20 products in the FDA NDC directory, labeler code 0126

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Colgate Oral Pharmaceuticals, Inc. (labeler code 0126) lists 20 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 14 prescription drugs, 5 over the counter drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on July 1, 2023.

The request: Watch Colgate Oral Pharmaceuticals, Inc. (FDA labeler code 0126): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
0126
Products in commercial distribution
20
Packages
23
Finished drugs by generic name
5
Prescription products
14
Over the counter products
5
Flagged as original packager
19 of 19 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
January 1, 1990
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs1260%
Over the counter monograph drugs525%
Generic drugs (ANDA)210%
Drugs for further processing15%

Products by type

TypeProductsShare
Prescription drugs1470%
Over the counter drugs525%
Drugs for further processing15%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Gel, dentifrice735%
Rinse630%
Paste, dentifrice630%
Mouthwash15%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
PreviDent 5000 Kids0126-0311Paste, dentifriceOther unapproved drugsJuly 1, 2023
Periogard Alcohol Free0126-0282RinseGeneric drugs (ANDA)October 4, 2021
Periogard Alcohol Free0126-0272RinseGeneric drugs (ANDA)November 18, 2020
PreviDent OrthoDefense0126-0289Paste, dentifriceOther unapproved drugsMarch 4, 2019
Hydrogen peroxide0126-0084RinseDrugs for further processingJanuary 1, 2017
PreviDent Alcohol Free0126-0033MouthwashOther unapproved drugsJune 13, 2016
PreviDent 5000 Booster Plus Spearmint0126-0074Paste, dentifriceOther unapproved drugsMarch 1, 2015
PreviDent 5000 Booster Plus Fruitastic0126-0072Paste, dentifriceOther unapproved drugsMarch 1, 2015
PreviDent Very Berry0126-0288Gel, dentifriceOther unapproved drugsAugust 29, 2012
PreviDent 5000 Plus Spearmint0126-0287Paste, dentifriceOther unapproved drugsAugust 29, 2012
PreviDent 5000 Plus Fruitastic0126-0286Paste, dentifriceOther unapproved drugsAugust 29, 2012
PreviDent Fresh Mint0126-0088Gel, dentifriceOther unapproved drugsAugust 29, 2012
PreviDent 5000 Enamel Protect0126-0022Gel, dentifriceOther unapproved drugsMarch 30, 2011
Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Gushing Grape Fluoride0126-0034RinseOver the counter monograph drugsFebruary 15, 2011
Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Mint Fluoride0126-0032RinseOver the counter monograph drugsJanuary 12, 2011
PreviDent 5000 Sensitive0126-0070Gel, dentifriceOther unapproved drugsJuly 6, 2009
PreviDent 5000 Dry Mouth0126-0016Gel, dentifriceOther unapproved drugsJuly 6, 2009
Peroxyl Mouth Sore Mild Mint0126-0083RinseOver the counter monograph drugsJanuary 1, 2009
Gel-Kam Mint0126-0192Gel, dentifriceOver the counter monograph drugsJanuary 1, 1990
Gel-Kam Fruit and Berry0126-0165Gel, dentifriceOver the counter monograph drugsJanuary 1, 1990

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.