Numotizine Ointment
Product Images NDC 10546-100

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Numotizine (NDC 10546-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hobart Laboratories, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label

NUMOTIZINE 1.25 g/100g ointment, a topical analgesic containing menthol, from Hobart Laboratories, Inc. The label displays drug facts including active ingredient menthol and usage instructions for temporary relief of muscle pain, soreness, stiffness, and arthritis. The product net weight is 3.5 oz (99 grams). Manufacturer contact information and warnings for external use appear on the label.*

FDA Label Image

Label2

NUMOTIZINE ointment with 1.25% menthol topical analgesic, labeled for temporary relief of pain and soreness. The label shows a net weight of 3.5 oz (99 grams) and lists Hobart Laboratories, Inc. as the manufacturer. Packaging features drug facts, warnings for external use only, dosage directions, uses, and a barcode.*

FDA Label Image

Numotizine8 (Numotizine8)

NUMOTIZINE ointment with 1.25% menthol as the active ingredient. This 8 oz (228 grams) topical analgesic ointment is produced by Hobart Laboratories, Inc., Bemidji, MN. The label includes directions for application and warnings for external use, covering details on use, storage, and precautions.*

FDA Label Image

Numotizinecarton (Numotizinecarton)

NUMOTIZINE ointment packaging label featuring the brand name in large blue letters. The label includes warnings for external use only and advises avoiding contact with eyes and mucous membranes. Manufactured by Hobart Laboratories, Inc., the net weight is 8 oz (228 grams). The label displays yellow and white stripes with blue text and logos.*

FDA Label Image

Numotizinecartona (Numotizinecartona)

Drug Facts and directions panel for NUMOTIZINE ointment with 1.25% menthol. The panel lists menthol as the active ingredient and describes its purpose as a topical analgesic. Inactive ingredients include clay, color, fragrance of guaiacol, methyl guaiacol, oil of wintergreen, and polyols. Usage instructions and warnings for topical application to relieve muscle pain and inflammation are included.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.