Register entry
- Registered sites
- 0
- Active NDC listings
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
33 active NDC listings: 3 human otc drug. By marketing category: OTC MONOGRAPH DRUG 3.
| Dosage form | NDCs |
|---|---|
| cream | 2 |
| lotion | 1 |
| Route | NDCs |
|---|---|
| topical | 3 |
| Labeller name on the listing | NDCs |
|---|---|
| lather, inc. | 3 |
Catalogue
Marketed products
3| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| LATHER- DAILY DEFENSE MINERAL SPF 50 | ZINC OXIDE | cream, topical | 77394-202OTC MONOGRAPH DRUG |
| LATHER- DAILY DEFENSE MINERAL SPF 50 BODY SUNSCREEN | Zinc Oxide | cream, topical | 77394-203OTC MONOGRAPH DRUG |
| Lather Daily Defense Mineral SPF 45 Facial Sunscreen | Zinc Oxide | lotion, topical | 77394-204OTC MONOGRAPH DRUG |
Compare
Other companies listing zinc oxide
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- Kenvue Brands LLC7 sites · 564 NDC
- BASF Corporation6 sites · 24 NDC
- Symrise, Inc.5 sites · 28 NDC
- Church & Dwight Co., Inc.4 sites · 157 NDC
- Cosmetic Solutions Holdings, LLC4 sites · 25 NDC
- Beiersdorf AG3 sites · 107 NDC
- Croda Europe Ltd.3 sites · 51 NDC
Enquiry
Common questions
- Is Lather, Inc. FDA approved?
- Lather, Inc. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Lather, Inc. make?
- 3 products are listed under Lather, Inc. in the openFDA NDC Directory, most often as cream; lotion. 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.