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Data / Drug companies / Medical Products Laboratories, Inc.

Medical Products Laboratories, Inc.: 14 products in the FDA NDC directory, labeler code 10733

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

Medical Products Laboratories, Inc. (labeler code 10733) lists 14 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 11 over the counter drugs, 2 prescription drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on December 8, 2024.

The request: Watch Medical Products Laboratories, Inc. (FDA labeler code 10733): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
10733
Products in commercial distribution
14
Packages
14
Finished drugs by generic name
4
Prescription products
2
Over the counter products
11
Flagged as original packager
12 of 12 products that carry the flag
Started marketing in the last 12 months
0
Products with a marketing end date set
1
Earliest marketing start
June 1, 1938
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 drugs1178.6%
Other unapproved drugs214.3%
Drugs for further processing17.1%

Products by type

TypeProductsShare
Over the counter drugs1178.6%
Prescription drugs214.3%
Drugs for further processing17.1%

Drugs it lists

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

DrugProductsCompanies listing it
Benzocaine10110
Aluminium chloride hexahydrate11
Salicylic acid and benzocaine11
Witch hazel163

Dosage forms

Dosage formProductsShare
Gel857.1%
Ointment214.3%
Solution214.3%
Patch17.1%
Liquid17.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Benzocaine10733-802SolutionDrugs for further processingDecember 8, 2024
Topicale Xtra10733-175GelOver the counter monograph drugsAugust 22, 2022
Topicale Xtra10733-176GelOver the counter monograph drugsAugust 17, 2022
Topicale Xtra10733-174GelOver the counter monograph drugsJuly 29, 2022
Witch Hazel10733-801LiquidOver the counter monograph drugsJanuary 29, 2021
Topicale10733-173PatchOver the counter monograph drugsMay 6, 2019
Topicale10733-169GelOver the counter monograph drugsApril 1, 2019
Topicale10733-171GelOver the counter monograph drugsMarch 5, 2019
Topicale10733-170GelOver the counter monograph drugsMarch 5, 2019
Topicale10733-167GelOver the counter monograph drugsMarch 5, 2019
Topicale10733-166GelOver the counter monograph drugsMarch 5, 2019
Topicale10733-162OintmentOver the counter monograph drugsMarch 5, 2019
Lumicain10733-412SolutionOther unapproved drugsSeptember 29, 2010
Salinocaine10733-415OintmentOther unapproved drugsJune 1, 1938

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.