Is Medical Products Laboratories, Inc. FDA approved?

Medical Products Laboratories, Inc. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Medical Products Laboratories, Inc.'s drugs manufactured?

The FDA register lists Philadelphia, PA. Registered operations: analytical testing, labelling, finished drug manufacture, packaging, relabelling, repackaging.

What drugs does Medical Products Laboratories, Inc. make?

13 products are listed under Medical Products Laboratories, Inc. in the openFDA NDC Directory, most often as gel; ointment; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Medical Products Laboratories, Inc.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 13
Labeller names: 2
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1Relabelling1Repackaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Medical Products Laboratories, Inc.	9990 Global Road, Philadelphia, Pennsylvania (PA) 19115, United States (USA)	Analytical testing, Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging	2513595002290302

Catalogue

Drug listings by form and route

13 active NDC listings: 11 human otc drug, 2 human prescription drug. By marketing category: OTC MONOGRAPH DRUG 11, UNAPPROVED DRUG OTHER 2.

Dosage form	NDCs
gel	8
ointment	2
liquid	1
patch	1
solution	1

Route	NDCs
oral	10
topical	3

Labeller name on the listing	NDCs
medical products laboratories, inc.	11
medical products laboratories,inc.	2

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Salinocaine	salicylic acid and benzocaine	ointment, topical	10733-415UNAPPROVED DRUG OTHER
Topicale	Benzocaine	ointment, oral	10733-162OTC MONOGRAPH DRUG
Topicale	Benzocaine	gel, oral	10733-166OTC MONOGRAPH DRUG
Topicale	Benzocaine	gel, oral	10733-167OTC MONOGRAPH DRUG
Topicale	Benzocaine	gel, oral	10733-169OTC MONOGRAPH DRUG
Topicale	Benzocaine	gel, oral	10733-170OTC MONOGRAPH DRUG
Topicale	Benzocaine	gel, oral	10733-171OTC MONOGRAPH DRUG
Topicale	Benzocaine	patch, oral	10733-173OTC MONOGRAPH DRUG
Topicale Xtra	Benzocaine	gel, oral	10733-174OTC MONOGRAPH DRUG
Topicale Xtra	Benzocaine	gel, oral	10733-175OTC MONOGRAPH DRUG
Topicale Xtra	Benzocaine	gel, oral	10733-176OTC MONOGRAPH DRUG
Witch Hazel	Witch Hazel	liquid, topical	10733-801OTC MONOGRAPH DRUG
lumicain	Aluminium Chloride Hexahydrate	solution, topical	10733-412UNAPPROVED DRUG OTHER

Neighbours

Registered in the same town

Catalent Pharma Solutions Inc.Philadelphia, PA
AstraZeneca PLCPhiladelphia, PA
Frontida BioPharm, LLCPhiladelphia, PA
Iovance Biotherapeutics, Inc.Philadelphia, PA
Premier Dental Products CompanyPhiladelphia, PA
Spark Therapeutics, Inc.Philadelphia, PA
Trustees of the University of PennsylvaniaPhiladelphia, PA
USWM CT, LLCPhiladelphia, PA

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Enquiry

Common questions

Is Medical Products Laboratories, Inc. FDA approved?: Medical Products Laboratories, Inc. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Medical Products Laboratories, Inc.'s drugs manufactured?: The FDA register lists Philadelphia, PA. Registered operations: analytical testing, labelling, finished drug manufacture, packaging, relabelling, repackaging.
What drugs does Medical Products Laboratories, Inc. make?: 13 products are listed under Medical Products Laboratories, Inc. in the openFDA NDC Directory, most often as gel; ointment; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.