Is Solesence, Inc. FDA approved?

Solesence, 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.

What drugs does Solesence, Inc. make?

9 products are listed under Solesence, Inc. in the openFDA NDC Directory, most often as powder; lotion; suspension. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Solesence, Inc.

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

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Registered sites: 1
Active NDC listings: 9
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Active ingredient (API) manufacture1Finished drug manufacture1Packaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Solesence, Inc.	400 W Crossroads Pkwy, Bolingbrook, Illinois (IL) 60440, United States (USA)	Active ingredient (API) manufacture, Finished drug manufacture, Packaging	3003574860118812921

Catalogue

Drug listings by form and route

9 active NDC listings: 7 bulk ingredient, 2 human otc drug. By marketing category: BULK INGREDIENT 7, OTC MONOGRAPH DRUG 2.

Dosage form	NDCs
powder	5
lotion	2
suspension	2

Route	NDCs
topical	2

Labeller name on the listing	NDCs
solesence, inc.	9

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Riversol Tinted Lip Oil - Poppy	Zinc Oxide	lotion, topical	63931-8421OTC MONOGRAPH DRUG
Riversol Tinted Lip Oil - Rosewood	Zinc Oxide	lotion, topical	63931-2116OTC MONOGRAPH DRUG
-	Solesence TM-S1	powder	63931-1567BULK INGREDIENT
-	Titanium Dioxide	powder	63931-1557BULK INGREDIENT
-	Zinc Oxide	powder	63931-1729BULK INGREDIENT
-	Zinc Oxide	powder	63931-4333BULK INGREDIENT
-	Zinc Oxide	suspension	63931-4425BULK INGREDIENT
-	Zinc Oxide	suspension	63931-4489BULK INGREDIENT
-	Zinc Oxide (USP)	powder	63931-4238BULK INGREDIENT

Neighbours

Registered in the same town

Craig SmithBolingbrook, IL
2XL CorporationBolingbrook, IL

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Enquiry

Common questions

Is Solesence, Inc. FDA approved?: Solesence, 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 Solesence, Inc.'s drugs manufactured?: The FDA register lists Bolingbrook, IL. Registered operations: active ingredient (API) manufacture, finished drug manufacture, packaging.
What drugs does Solesence, Inc. make?: 9 products are listed under Solesence, Inc. in the openFDA NDC Directory, most often as powder; lotion; suspension. 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.