Skip to the page

Data / Drug companies / Professional Disposables International, Inc.

Professional Disposables International, Inc.: 17 products in the FDA NDC directory, labeler code 10819

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

Professional Disposables International, Inc. (labeler code 10819) lists 17 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 17 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on June 22, 2026.

The request: Watch Professional Disposables International, Inc. (FDA labeler code 10819): 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
10819
Products in commercial distribution
17
Packages
22
Finished drugs by generic name
7
Prescription products
0
Over the counter products
17
Flagged as original packager
13 of 13 products that carry the flag
Started marketing in the last 12 months
2
Products with a marketing end date set
2
Earliest marketing start
January 1, 1972
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 drugs1376.5%
New drug applications (NDA)423.5%

Products by type

TypeProductsShare
Over the counter drugs17100%

Drugs it lists

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

DrugProductsCompanies listing it
Alcohol6293
Chlorhexidine gluconate and isopropyl alcohol43
Povidone iodine usp, 10% w/w21
Providone iodine21
Povidone iodine114
Povidone-iodine158
Instant hand sanitizing wipes11

Dosage forms

Dosage formProductsShare
Cloth741.2%
Swab423.5%
Solution423.5%
Stick211.8%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
PVP-I Prep Pad10819-3801SwabOver the counter monograph drugsJune 22, 2026
Profend Nasal Antiseptic Kit10819-3889SwabOver the counter monograph drugsMarch 17, 2026
Povidone-Iodine Swabstick10819-3800StickOver the counter monograph drugsMay 15, 2025
Prevantics Swabstick10819-4077SolutionNew drug applications (NDA)June 1, 2020
Sani Professional Hands Instant Sanitizing Wipes10819-6007ClothOver the counter monograph drugsMarch 1, 2020
Sani Professional Hands Instant Sanitizing Wipes10819-6006ClothOver the counter monograph drugsMarch 1, 2020
Sani Professional Hands Instant Sanitizing Wipes10819-6008ClothOver the counter monograph drugsJanuary 1, 2020
Prevantics Maxi Swabstick10819-4076SolutionNew drug applications (NDA)January 1, 2020
Profend Nasal Decolonization10819-3888SwabOver the counter monograph drugsFebruary 16, 2018
PDI Sani Hands10819-3918ClothOver the counter monograph drugsApril 1, 2016
PDI Sani-Hands Instant Hand Sanitizing Wipes10819-3917ClothOver the counter monograph drugsMarch 24, 2014
PDI Sani-Hands Instant Hand Sanitizing Wipes10819-3916ClothOver the counter monograph drugsJanuary 1, 2014
Prevantics Swab10819-1080SolutionNew drug applications (NDA)January 15, 2013
Prevantics Swab10819-1080SolutionNew drug applications (NDA)January 15, 2013
PVP Iodine Prep Swabstick Ones and Threes10819-3885StickOver the counter monograph drugsJanuary 1, 1978
PVP Iodine Prep Pad Medium and Large10819-3883SwabOver the counter monograph drugsJanuary 1, 1978
PDI Alcohol Prep Pad Sterile Large and Medium10819-3914ClothOver the counter monograph drugsJanuary 1, 1972

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.