Lather, Inc.
Lather, Inc. is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human otc drug products.
About Lather, Inc.
Lather, Inc. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by ZINC OXIDE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: helps prevent, sun protection, measures see, directions decreases, risk skin, aging cause. Use the table below to identify a specific product, then open it for full indications, dosage and warnings as filed with the FDA.
Active ingredients in this portfolio
| Active ingredient | Products |
|---|---|
| ZINC OXIDE | 1 |
Dosage forms and routes
| Dosage form | Products | Route | Products |
|---|---|---|---|
| — | — | TOPICAL | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
FDA drug products from Lather, Inc.
| Brand name | Generic | Type | Route |
|---|---|---|---|
| Lather Daily Defense Mineral SPF 45 Facial Sunscreen | ZINC OXIDE | HUMAN OTC DRUG | TOPICAL |
Frequently asked questions
How many FDA drug products does Lather, Inc. make?
1 FDA drug label records name Lather, Inc. as the manufacturer, covering 1 distinct active ingredients.
What active ingredients does Lather, Inc. produce?
The most frequent active ingredients in this portfolio are ZINC OXIDE.
Are Lather, Inc. products prescription or over-the-counter?
The largest share of this company’s labels are human otc drug products; check each product page for its own marketing status.
Does this page list prices or where to buy?
No. This is a labelling reference built from FDA data. It does not sell, price or recommend any medicine.
Labelling data reproduced from FDA Structured Product Labelling for identification only. This site does not sell, price or recommend any medicine.