Register entry
- Registered sites
- 1
- Drug products
- 12
- Live patents
- 0
- Countries
- 1
- Base
- United States
Authorisation
Registered operations
What the FDA has registered these sites to do. This is the regulatory record, not a marketing claim.
LabellingFinished drug manufacturePackagingRelabellingRepackaging
Sites
Facilities
1| Site | Location | Operations | FEI |
|---|---|---|---|
| Rnv LLC | Miami Lakes, FLUnited States | Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging | 3026274805 |
Catalogue
Marketed products
12Showing 12 of 12.
| Brand | Generic name | Form | Category |
|---|---|---|---|
| REVASOL CHILDRENS ALLERGY | DIPHENHYDRAMINE HCL | LIQUID | OTC MONOGRAPH DRUG |
| REVASOL DAYTIME COLD AND FLU | Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride | LIQUID | OTC MONOGRAPH DRUG |
| REVASOL NIGHTTIME COLD AND FLU | Acetaminophen, Dextromethorphan HBr and Doxylamine succinate | LIQUID | OTC MONOGRAPH DRUG |
| REVASOL SLEEP AID | Diphenhydramine HCl | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Acetaminophen Suspension | Acetaminophen | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Acetaminophen Suspension Dye Free | Acetaminophen | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Peptic Relief | Bismuth subsalicylate | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Tussin | Guaifenesin | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Tussin DM Cough Suppressant Expectorant | Dextromethorphan HBr, Guaifenesin | LIQUID | OTC MONOGRAPH DRUG |
| Revasol Tussin DM Max with Honey | Dextromethorphan HBr and Guaifenesin | LIQUID | OTC MONOGRAPH DRUG |
| XL-3 Day Time | acetaminophen, dextromethorphan HBr, Phenylephrine HCl | LIQUID | OTC MONOGRAPH DRUG |
| XL-3 Night Time | acetaminophen, dextromethorphan HBr, Doxylamine Succinate | LIQUID | OTC MONOGRAPH DRUG |
Provenance
Facility and operations data from the FDA Drug Establishments Current Registration Site. Product data from the openFDA National Drug Code Directory. Patent and exclusivity data from the FDA Orange Book. Shortage data from the FDA drug shortage database. Contact details the FDA publishes for registered establishments are deliberately not reproduced here. This entry is compiled from public records and has not been claimed by the company.