Register entryRepackager / relabeller
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- United States
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Boxout, LLC | 6333 Hudson Crossing Parkway, Hudson, Ohio (OH) 44236, United States (USA) | Packaging | 3008492870066689993 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| BodyMed Alcohol Prep Pad | Alcohol Prep Pad | swab, topical | 82308-001OTC MONOGRAPH DRUG |
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Enquiry
Common questions
- Is Boxout, LLC FDA approved?
- Boxout, LLC 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 Boxout, LLC's registered sites?
- The FDA register lists Hudson, OH. Registered operations: packaging.
- What drugs does Boxout, LLC make?
- 1 product is listed under Boxout, LLC in the openFDA NDC Directory, most often as swab. 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.