Is NOMAX, INC FDA approved?

NOMAX, 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 NOMAX, INC's drugs manufactured?

The FDA register lists Saint Louis, MO. Registered operations: finished drug manufacture.

What drugs does NOMAX, INC make?

16 products are listed under NOMAX, INC in the openFDA NDC Directory, most often as tablet, effervescent; strip; gel. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

NOMAX, INC

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

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Registered sites: 1
Active NDC listings: 16
Labeller names: 3
Live patents: 0
Countries: 1
Base: United States

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Nomax, INCRegistrant: NOMAX, INC	9735 Green Park Industrial Drive, Saint Louis, Missouri (MO) 63123, United States (USA)	Finished drug manufacture	1937310103220273

Catalogue

Drug listings by form and route

16 active NDC listings: 12 human prescription drug, 4 human otc drug. By marketing category: UNAPPROVED DRUG OTHER 12, OTC MONOGRAPH DRUG 4.

Dosage form	NDCs
tablet, effervescent	8
strip	4
gel	1
solution	1
solution/ drops	1
spray	1

Route	NDCs
oral	8
ophthalmic	5
topical	3

Labeller name on the listing	NDCs
nomax inc.	12
nomax, inc.	3
nomax inc	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer	Alcohol	gel, topical	51801-437OTC MONOGRAPH DRUG
Amcon Labs Hand Sanitizer Instant Foam Sanitizer with Alcohol	Alcohol	solution, topical	51801-366OTC MONOGRAPH DRUG
Amcon Labs Hand Sanitizer Light Cleansing	Alcohol	spray, topical	51801-779OTC MONOGRAPH DRUG
Dry Eye Test	Fluorescein Sodium	strip, ophthalmic	51801-008UNAPPROVED DRUG OTHER
Effer-K 10 mEq Cherry Vanilla	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-014UNAPPROVED DRUG OTHER
Effer-K 10 mEq Unflavored	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-013UNAPPROVED DRUG OTHER
Effer-K 20 mEq Orange Cream	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-012UNAPPROVED DRUG OTHER
Effer-K 20 mEq Unflavored	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-011UNAPPROVED DRUG OTHER
Effer-K Cherry Berry	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-006UNAPPROVED DRUG OTHER
Effer-K Lemon Citrus	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-005UNAPPROVED DRUG OTHER
Effer-K Orange	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-001UNAPPROVED DRUG OTHER
Effer-K Unflavored	POTASSIUM BICARBONATE	tablet, effervescent, oral	51801-007UNAPPROVED DRUG OTHER
GloStrips	Fluorescein Sodium	strip, ophthalmic	51801-003UNAPPROVED DRUG OTHER
GloStrips	Rose Bengal Sodium	strip, ophthalmic	51801-004UNAPPROVED DRUG OTHER
GloStrips	Fluorescein Sodium	strip, ophthalmic	51801-009UNAPPROVED DRUG OTHER
Viva Hydration Boost	Glycerin	solution/ drops, ophthalmic	51801-016OTC MONOGRAPH DRUG

Neighbours

Registered in the same town

Sigma-Aldrich CorporationSaint Louis, MO · 2 sites
Missouri Analytical Laboratories, Inc.Saint Louis, MO · 2 sites
Patheon Manufacturing Services LLCSaint Louis, MO
Jerry JostSaint Louis, MO
Lafayette IndustriesSaint Louis, MO
CEE-KAY SUPPLY, INC.SAINT LOUIS, MO
Chemisphere CorporationSaint Louis, MO
Heartland Industries IncorporatedSaint Louis, MO

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Enquiry

Common questions

Is NOMAX, INC FDA approved?: NOMAX, 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 NOMAX, INC's drugs manufactured?: The FDA register lists Saint Louis, MO. Registered operations: finished drug manufacture.
What drugs does NOMAX, INC make?: 16 products are listed under NOMAX, INC in the openFDA NDC Directory, most often as tablet, effervescent; strip; 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.