Is CHEMCO CORPORATION FDA approved?

CHEMCO CORPORATION 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 CHEMCO CORPORATION's drugs manufactured?

The FDA register lists Hialeah, FL. Registered operations: finished drug manufacture.

What drugs does CHEMCO CORPORATION make?

16 products are listed under CHEMCO CORPORATION in the openFDA NDC Directory, most often as liquid; cream; gel. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

CHEMCO CORPORATION

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

Request a quote Claim this profile

Registered sites: 1
Active NDC listings: 16
Labeller names: 4
Live patents: 0
Countries: 1
Base: United States

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Chemco CorporationRegistrant: CHEMCO CORPORATION	4920 NW 165th St, Hialeah, Florida (FL) 33014, United States (USA)	Finished drug manufacture	1042599032495954

Catalogue

Drug listings by form and route

16 active NDC listings: 16 human otc drug. By marketing category: OTC MONOGRAPH DRUG 16.

Dosage form	NDCs
liquid	5
cream	4
gel	3
lotion	2
spray	2

Route	NDCs
topical	16

Labeller name on the listing	NDCs
chemco corporation	10
chemco corporation	3
chemco products company	2
chemco	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
AB 3000	Benzalkonium Chloride	liquid, topical	63039-1006OTC MONOGRAPH DRUG
ANTIFUNGAL	Undecylenic Acid	liquid, topical	49283-250OTC MONOGRAPH DRUG
Antibacterial Foam Hand Wash	CHLOROXYLENOL	liquid, topical	63039-1005OTC MONOGRAPH DRUG
COOLING PAIN RELIEF	MENTHOL, CAMPHOR	gel, topical	49283-581OTC MONOGRAPH DRUG
E-2 Food Processing Foam Hand Wash	BENZALKONIUM CHLORIDE	liquid, topical	63039-1002OTC MONOGRAPH DRUG
FOOTSPA PEDI	ALCOHOL	spray, topical	49283-702OTC MONOGRAPH DRUG
FOOTSPA PEDI	ALCOHOL	spray, topical	49283-707OTC MONOGRAPH DRUG
GELLE-N-DETOX - LAVENDER AND ROSEMARY MASSAGE	BENZALKONIUM CHLORIDE	lotion, topical	49283-001OTC MONOGRAPH DRUG
GELLE-N-DETOX ICE MINT AND EUCALYPTUS MASSAGE	BENZALKONIUM CHLORIDE	lotion, topical	49283-110OTC MONOGRAPH DRUG
HEATING PAIN RELIEF	METHYL SALICYLATE, MENTHOL	cream, topical	49283-579OTC MONOGRAPH DRUG
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	cream, topical	49283-580OTC MONOGRAPH DRUG
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	cream, topical	49283-582OTC MONOGRAPH DRUG
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	gel, topical	49283-583OTC MONOGRAPH DRUG
Menthol, Camphor	Menthol, Camphor	cream, topical	49283-576OTC MONOGRAPH DRUG
ULTRA RELIEF	MENTHOL, CAMPHOR	gel, topical	49283-578OTC MONOGRAPH DRUG
Undecylenic Acid	Undecylenic Acid	liquid, topical	49283-025OTC MONOGRAPH DRUG

Neighbours

Registered in the same town

Hair Sense Holdings LLCHialeah, FL

Compare

Comparable companies in United States

Hahnemann Laboratories, Inc. dba Alpine Pharmaceuticals1 site · 4,853 NDC
NuCare Pharmaceuticals,Inc.1 site · 1,393 NDC
Greer Laboratories, Inc.1 site · 1,328 NDC
ASCLEMED USA INC. DBA ENOVACHEM1 site · 789 NDC
Golden State Medical Supply Inc.1 site · 670 NDC
Rising Pharma Holdings, Inc.1 site · 532 NDC
HF Acquisition Co LLC1 site · 363 NDC
ANI Pharmaceuticals, Inc.1 site · 299 NDC
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1 site · 273 NDC
Newton Laboratories, Inc.1 site · 271 NDC

Enquiry

Common questions

Is CHEMCO CORPORATION FDA approved?: CHEMCO CORPORATION 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 CHEMCO CORPORATION's drugs manufactured?: The FDA register lists Hialeah, FL. Registered operations: finished drug manufacture.
What drugs does CHEMCO CORPORATION make?: 16 products are listed under CHEMCO CORPORATION in the openFDA NDC Directory, most often as liquid; cream; gel. 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.