Is KC Pharmaceuticals, Inc. FDA approved?

KC Pharmaceuticals, 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 KC Pharmaceuticals, Inc.'s drugs manufactured?

The FDA register lists Pomona, CA. Registered operations: labelling, finished drug manufacture, packaging.

What drugs does KC Pharmaceuticals, Inc. make?

14 products are listed under KC Pharmaceuticals, Inc. in the openFDA NDC Directory, most often as solution/ drops; solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

KC Pharmaceuticals, Inc.

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

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Registered sites: 1
Active NDC listings: 14
Labeller names: 4
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Labelling1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
KC Pharmaceuticals, Inc.	3201 Producer Way, Pomona, California (CA) 91768-3236, United States (USA)	Labelling, Finished drug manufacture, Packaging	2026940174450460

Catalogue

Drug listings by form and route

14 active NDC listings: 14 human otc drug. By marketing category: OTC MONOGRAPH DRUG 14.

Dosage form	NDCs
solution/ drops	10
solution	4

Route	NDCs
ophthalmic	14

Labeller name on the listing	NDCs
kc pharmaceuticals, inc.	9
k.c. pharmaceuticals, inc.	2
kc pharmaceuticals, inc	2
kc pharmaceuticals	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Artificial Tears	polyvinyl alcohol, povidone	solution/ drops, ophthalmic	55651-008OTC MONOGRAPH DRUG
Artificial Tears Lubricant Eye Drops	Glycerin, Hypromellose, Polyethylene glycol 400	solution/ drops, ophthalmic	55651-115OTC MONOGRAPH DRUG
Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	solution/ drops, ophthalmic	55651-105OTC MONOGRAPH DRUG
Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM	solution/ drops, ophthalmic	55651-510OTC MONOGRAPH DRUG
Medics Choice Eye Drops Advanced	tetrahydrozoline hydrochloride, polyethylene glycol 400, dextran 70, povidone	solution/ drops, ophthalmic	55651-025OTC MONOGRAPH DRUG
Medics Choice Eye Drops Maximum Redness Relief	glycerin, naphazoline hydrochloride	solution, ophthalmic	55651-059OTC MONOGRAPH DRUG
Medics Choice Eye Drops Original Redness Reliever	tetrahydrozoline hydrochloride	solution/ drops, ophthalmic	55651-005OTC MONOGRAPH DRUG
Medics Choice Eye Drops Seasonal Relief	tetrahydrozoline hydrochloride, zinc sulfate	solution/ drops, ophthalmic	55651-024OTC MONOGRAPH DRUG
Medics Choice Fresh and Soothe	CARBOXYMETHYLCELLULOSE SODIUM, Glycerin	solution/ drops, ophthalmic	55651-200OTC MONOGRAPH DRUG
Medics Choice Fresh and Soothe Lubricant Eye Drops	Polyethylene glycol 400, Propylene glycol	solution/ drops, ophthalmic	55651-999OTC MONOGRAPH DRUG
Medics Choice Lubricant Eye Drops	carboxymethylcellulose sodium	solution, ophthalmic	55651-030OTC MONOGRAPH DRUG
Medics Choice Soothing Eye Wash	Purified water	solution, ophthalmic	55651-555OTC MONOGRAPH DRUG
Original Redness Reliever	Tetrahydrolizine HCL	solution/ drops, ophthalmic	55651-063OTC MONOGRAPH DRUG
Redness and Dry Eye Relief	Glycerin, Naphazoline hydrochloride	solution, ophthalmic	55651-620OTC MONOGRAPH DRUG

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Enquiry

Common questions

Is KC Pharmaceuticals, Inc. FDA approved?: KC Pharmaceuticals, 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 KC Pharmaceuticals, Inc.'s drugs manufactured?: The FDA register lists Pomona, CA. Registered operations: labelling, finished drug manufacture, packaging.
What drugs does KC Pharmaceuticals, Inc. make?: 14 products are listed under KC Pharmaceuticals, Inc. in the openFDA NDC Directory, most often as solution/ drops; solution. 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.