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

2

2 active NDC listings: 2 human otc drug. By marketing category: OTC MONOGRAPH DRUG 2.

Dosage formNDCs
cream2
RouteNDCs
topical2
Labeller name on the listingNDCs
herbalife international of america inc.1
herbalife international of america, inc.1
Catalogue

Marketed products

2
BrandGeneric nameForm / routeNDC
Herbalife Herbal Aloe Face and Body Mineral Sunscreen Broad Spectrum SPF 30Zinc Oxidecream, topical51785-922OTC MONOGRAPH DRUG
Herbalife SKIN Protective Moisturizer Broad Spectrum SPF 30 Mineral SunscreenZinc Oxidecream, topical51785-900OTC MONOGRAPH DRUG
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Other companies listing zinc oxide

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.