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Data / Drug companies / C.B. Fleet Company, Inc.

C.B. Fleet Company, Inc.: 23 products in the FDA NDC directory, labeler code 0132

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

C.B. Fleet Company, Inc. (labeler code 0132) lists 23 products in the FDA National Drug Code Directory, covering 9 finished drugs by generic name. By type: 23 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on June 21, 2024.

The request: Watch C.B. Fleet Company, Inc. (FDA labeler code 0132): 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
0132
Products in commercial distribution
23
Packages
35
Finished drugs by generic name
9
Prescription products
0
Over the counter products
23
Flagged as original packager
21 of 21 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
March 10, 1953
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs23100%

Products by type

TypeProductsShare
Over the counter drugs23100%

Drugs it lists

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

DrugProductsCompanies listing it
Zinc oxide5595
Glycerin456
Sodium phosphate, dibasic and sodium phosphate, monobasic31
Simethicone386
Docusate sodium279
Mineral oil234
Bisacodyl260
Magnesium hydroxide141
Dimethicone169

Dosage forms

Dosage formProductsShare
Liquid521.7%
Enema521.7%
Cream313%
Ointment28.7%
Capsule, gelatin coated28.7%
Capsule, liquid filled28.7%
Suppository14.3%
Tablet, chewable14.3%
Kit14.3%
Tablet, coated14.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Fleet0132-0402Capsule, liquid filledOver the counter monograph drugsJune 21, 2024
Fleet0132-0401Tablet, coatedOver the counter monograph drugsJune 21, 2024
Fleet0132-0400LiquidOver the counter monograph drugsApril 1, 2024
Boudreauxs Baby Shower Bundle0132-0327KitOver the counter monograph drugsFebruary 1, 2024
Pedia-Lax0132-0113LiquidOver the counter monograph drugsFebruary 28, 2023
Phazyme Ultimate0132-0222Capsule, liquid filledOver the counter monograph drugsMarch 13, 2022
Boudreauxs Butt Barrier0132-0326OintmentOver the counter monograph drugsMarch 1, 2022
Boudreauxs0132-0324OintmentOver the counter monograph drugsDecember 2, 2019
Pedia-Lax0132-0195LiquidOver the counter monograph drugsFebruary 1, 2019
Phazyme0132-0211Capsule, gelatin coatedOver the counter monograph drugsApril 1, 2014
Boudreauxs0132-0334CreamOver the counter monograph drugsFebruary 1, 2012
Boudreauxs0132-0333CreamOver the counter monograph drugsFebruary 1, 2012
Boudreauxs0132-0323CreamOver the counter monograph drugsFebruary 1, 2012
Phazyme0132-0208Capsule, gelatin coatedOver the counter monograph drugsFebruary 1, 2012
Pedia-Lax0132-0655Tablet, chewableOver the counter monograph drugsMarch 1, 2008
Pedia-Lax0132-0190LiquidOver the counter monograph drugsMarch 1, 2008
Fleet0132-0078EnemaOver the counter monograph drugsJune 25, 2004
Fleet0132-0185LiquidOver the counter monograph drugsJune 3, 2002
Fleet0132-0703EnemaOver the counter monograph drugsMay 10, 2002
Pedia-Lax0132-0202EnemaOver the counter monograph drugsMay 10, 2002
Fleet0132-0301EnemaOver the counter monograph drugsMay 1, 2002
Fleet0132-0075SuppositoryOver the counter monograph drugsNovember 1, 1984
Fleet0132-0201EnemaOver the counter monograph drugsMarch 10, 1953

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.