Skip to the page

Data / Drug companies / H E B

H E B: 37 products in the FDA NDC directory, labeler code 59640

H E B (labeler code 59640) lists 37 products in the FDA National Drug Code Directory, covering 20 finished drugs by generic name. By type: 37 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 7, 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
59640
Products in commercial distribution
37
Packages
45
Finished drugs by generic name
20
Prescription products
0
Over the counter products
37
Flagged as original packager
32 of 32 products that carry the flag
Started marketing in the last 12 months
16
Products with a marketing end date set
1
Earliest marketing start
May 1, 2018
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 drugs2464.9%
Generic drugs (ANDA)1232.4%
New drug applications (NDA)12.7%

Products by type

TypeProductsShare
Over the counter drugs37100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Liquid1027%
Solution718.9%
Tablet, film coated38.1%
Capsule, liquid filled25.4%
Lozenge25.4%
Tablet, multilayer, extended release25.4%
Suspension25.4%
Aerosol, powder12.7%
Capsule, delayed release12.7%
Spray12.7%
Patch12.7%
Gel12.7%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Omeprazole59640-699Capsule, delayed releaseGeneric drugs (ANDA)August 7, 2026
Benzalkonium Chloride59640-373LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-321LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-317LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-306LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-290LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium chloride59640-273LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium chloride59640-252LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-149LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-094LiquidOver the counter monograph drugsJuly 15, 2026
Benzalkonium Chloride59640-346LiquidOver the counter monograph drugsJuly 10, 2026
Clear anti itch59640-218LotionOver the counter monograph drugsJune 23, 2026
Gel Corn Remover59640-802PatchOver the counter monograph drugsMay 21, 2026
Triple Antibiotic59640-801OintmentOver the counter monograph drugsApril 2, 2026
Allergy Relief59640-090Capsule, liquid filledOver the counter monograph drugsMarch 12, 2026
Ibuprofen PM59640-020Capsule, liquid filledGeneric drugs (ANDA)March 12, 2026
Childrens cold and cough59640-200SolutionOver the counter monograph drugsNovember 4, 2025
Nicotine59640-151LozengeGeneric drugs (ANDA)August 12, 2025
Nicotine59640-099LozengeGeneric drugs (ANDA)August 12, 2025
Nighttime SEVERE59640-423SolutionOver the counter monograph drugsAugust 8, 2025
Daytime Severe59640-308SolutionOver the counter monograph drugsAugust 5, 2025
Arthritis pain reliever59640-198GelGeneric drugs (ANDA)April 22, 2025
Nasal59640-388SprayOver the counter monograph drugsApril 4, 2025
HEB Athlete Foot Antifungal59640-101Aerosol, powderOver the counter monograph drugsFebruary 14, 2025
Infants pain fever59640-766SuspensionOver the counter monograph drugsJuly 22, 2024

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.