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Data / Drug companies / P & L Development, LLC

P & L Development, LLC: 30 products in the FDA NDC directory, labeler code 49580

P & L Development, LLC (labeler code 49580) lists 30 products in the FDA National Drug Code Directory, covering 14 finished drugs by generic name. By type: 30 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on July 15, 2026.

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
49580
Products in commercial distribution
30
Packages
58
Finished drugs by generic name
14
Prescription products
0
Over the counter products
30
Flagged as original packager
29 of 29 products that carry the flag
Started marketing in the last 12 months
2
Products with a marketing end date set
3
Earliest marketing start
June 30, 2014
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 drugs30100%

Products by type

TypeProductsShare
Over the counter drugs30100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Liquid2376.7%
Suspension413.3%
Oil13.3%
Spray13.3%
Granule13.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Hydrogen Peroxide49580-0400LiquidOver the counter monograph drugsJuly 15, 2026
Isopropyl alcohol 91 percent49580-4162LiquidOver the counter monograph drugsJune 30, 2026
Tussin Cough Sugar Free49580-0834LiquidOver the counter monograph drugsJuly 31, 2024
Pain Relief49580-0821SuspensionOver the counter monograph drugsJuly 31, 2024
Pain Reliever49580-2880SuspensionOver the counter monograph drugsMarch 15, 2024
Nighttime Severe Cold and Cough49580-0502LiquidOver the counter monograph drugsApril 30, 2021
Severe cold and flu Nighttime49580-4160LiquidOver the counter monograph drugsMarch 26, 2021
Severe Cold and Cough Relief Daytime49580-0501LiquidOver the counter monograph drugsMarch 26, 2021
Severe Cold and Flu Relief Daytime49580-0415LiquidOver the counter monograph drugsMarch 26, 2021
Stomach Relief Regular Strength49580-0724LiquidOver the counter monograph drugsOctober 30, 2019
Stomach Relief Regular Strength49580-0624LiquidOver the counter monograph drugsSeptember 30, 2019
Stomach Relief Ultra Strength49580-0842LiquidOver the counter monograph drugsFebruary 28, 2019
Dye Free Pain Reliever Childrens49580-0685SuspensionOver the counter monograph drugsFebruary 28, 2018
Epsom Salt49580-0394GranuleOver the counter monograph drugsDecember 31, 2017
Sleep Aid NightTime49580-0314LiquidOver the counter monograph drugsAugust 31, 2016
Pain and Fever Childrens49580-0282SuspensionOver the counter monograph drugsMay 31, 2016
Severe cold and flu Nighttime49580-0416LiquidOver the counter monograph drugsAugust 31, 2015
Daytime Cold and Flu49580-0466LiquidOver the counter monograph drugsJune 30, 2015
Tussin DM Cough and Chest Congestion Adult49580-0385LiquidOver the counter monograph drugsMarch 31, 2015
Childrens Allergy49580-0292LiquidOver the counter monograph drugsMarch 31, 2015
Childrens Dye Free Allergy49580-0293LiquidOver the counter monograph drugsFebruary 28, 2015
Sore Throat ReadyInCase49580-0376SprayOver the counter monograph drugsNovember 30, 2014
Nighttime Cold and Flu ReadyInCase49580-0346LiquidOver the counter monograph drugsNovember 30, 2014
Night Time Cold and Flu ReadyInCase49580-0343LiquidOver the counter monograph drugsOctober 31, 2014
Witch Hazel ReadyInCase49580-0390LiquidOver the counter monograph drugsAugust 31, 2014

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