Register entry
Herbalife International of America, Inc.
Data as of · How to read this entry
- Registered sites
- 0
- Active NDC listings
- 2
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human otc drug. By marketing category: OTC MONOGRAPH DRUG 2.
| Dosage form | NDCs |
|---|---|
| cream | 2 |
| Route | NDCs |
|---|---|
| topical | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| herbalife international of america inc. | 1 |
| herbalife international of america, inc. | 1 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Herbalife Herbal Aloe Face and Body Mineral Sunscreen Broad Spectrum SPF 30 | Zinc Oxide | cream, topical | 51785-922OTC MONOGRAPH DRUG |
| Herbalife SKIN Protective Moisturizer Broad Spectrum SPF 30 Mineral Sunscreen | Zinc Oxide | cream, topical | 51785-900OTC MONOGRAPH DRUG |
Compare
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Enquiry
Common questions
- Is Herbalife International of America, Inc. FDA approved?
- Herbalife International of America, Inc. holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Herbalife International of America, Inc. make?
- 2 products are listed under Herbalife International of America, Inc. in the openFDA NDC Directory, most often as cream. 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.