GC America Inc.

1 FDA products 1 active ingredients HUMAN OTC DRUG

GC America Inc. is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human otc drug products.

About GC America Inc.

GC America Inc. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by SODIUM FLUORIDE. Most of these labels are human otc drug products. Labelling across this portfolio most often references: recommended indications, polishing procedures, part professionally, administered prophylaxis, treatment secondarily, paste plus, management tooth, sensitivity post-scaling. 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 1

Dosage forms and routes

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

FDA drug products from GC America Inc.

Brand nameGenericTypeRoute
MIPaste Plus Strawberry SODIUM FLUORIDE HUMAN OTC DRUG DENTAL

Frequently asked questions

How many FDA drug products does GC America Inc. make?
1 FDA drug label records name GC America Inc. as the manufacturer, covering 1 distinct active ingredients.

What active ingredients does GC America Inc. produce?
The most frequent active ingredients in this portfolio are SODIUM FLUORIDE.

Are GC America 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.