Project Noah Inc.
Project Noah Inc. is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human otc drug products.
About Project Noah Inc.
Project Noah Inc. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by SODIUM MONOFLUOROPHOSPHATE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: prevention dental. 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 |
|---|---|
| SODIUM MONOFLUOROPHOSPHATE | 1 |
Dosage forms and routes
| Dosage form | Products | Route | Products |
|---|---|---|---|
| — | — | ORAL | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
FDA drug products from Project Noah Inc.
| Brand name | Generic | Type | Route |
|---|---|---|---|
| Dr. Noah Kids Tooth | SODIUM MONOFLUOROPHOSPHATE | HUMAN OTC DRUG | ORAL |
Frequently asked questions
How many FDA drug products does Project Noah Inc. make?
1 FDA drug label records name Project Noah Inc. as the manufacturer, covering 1 distinct active ingredients.
What active ingredients does Project Noah Inc. produce?
The most frequent active ingredients in this portfolio are SODIUM MONOFLUOROPHOSPHATE.
Are Project Noah 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.