Brio Product Group LLC.

1 FDA products 1 active ingredients HUMAN OTC DRUG

Brio Product Group LLC. is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human otc drug products.

About Brio Product Group LLC.

Brio Product Group LLC. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by SODIUM FLUORIDE, POTASSIUM NITRATE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: helps protect, against cavities. 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 ingredientProducts
SODIUM FLUORIDE, POTASSIUM NITRATE 1

Dosage forms and routes

Dosage formProductsRouteProducts
— — DENTAL 1
— — — —
— — — —
— — — —
— — — —
— — — —

FDA drug products from Brio Product Group LLC.

Brand nameGenericTypeRoute
Ollie Fresh Mint SODIUM FLUORIDE, POTASSIUM NITRATE HUMAN OTC DRUG DENTAL

Frequently asked questions

How many FDA drug products does Brio Product Group LLC. make?
1 FDA drug label records name Brio Product Group LLC. as the manufacturer, covering 1 distinct active ingredients.

What active ingredients does Brio Product Group LLC. produce?
The most frequent active ingredients in this portfolio are SODIUM FLUORIDE, POTASSIUM NITRATE.

Are Brio Product Group LLC. 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.