Hobart Laboratories, Inc.

1 FDA products 1 active ingredients HUMAN OTC DRUG

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

About Hobart Laboratories, Inc.

Hobart Laboratories, Inc. is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by MENTHOL. Most of these labels are human otc drug products. Labelling across this portfolio most often references: topical analgesic, provides temporary, relief muscle, pain soreness, strains sprains, tendon injuries. 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
MENTHOL 1

Dosage forms and routes

Dosage formProductsRouteProducts
— — TOPICAL 1
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— — — —
— — — —
— — — —
— — — —

FDA drug products from Hobart Laboratories, Inc.

Brand nameGenericTypeRoute
NUMOTIZINE MENTHOL HUMAN OTC DRUG TOPICAL

Frequently asked questions

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

What active ingredients does Hobart Laboratories, Inc. produce?
The most frequent active ingredients in this portfolio are MENTHOL.

Are Hobart Laboratories, 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.