Numotizine Ointment
Product Images NDC 10546-100

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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

Label
This is a drug with the active ingredient of Menthol to be used topically as an analgesic to provide temporary pain relief for soreness and stiffness. The ointment should be spread from 1 to 4 inches on the affected area and then covered with cloth or a bandage or clothing. The drug includes ingredients like Guaiacol and oil of Wintergreen. The product should be removed with warm water before applying it again. If needed, the application can be repeated every 12 hours. For further information, visit www.numotizine.com or call 1-218-751-9505.*
FDA Label Image

Label2

Label2
Numotizine is a topical analgesic ointment that provides temporary relief for muscle pain, soreness, stiffness, strains, sprains, ligament and tendon injuries, and arthritis. The ointment should be spread 1/8" of an inch thick onto the skin and covered with a cloth or bandage to protect clothing. It should be removed with warm water before it is totally dry, usually after 8-12 hours. The ointment should be reapplied every 12 hours as needed. Stop using the ointment and consult a doctor if there is excessive irritation of the skin or persistent swelling. The product should be kept out of reach of children. Menthol is the active ingredient in Numotizine. The ointment weighs 3.5 oz (99 grams) and has been manufactured by Hobart Laboratories, Inc. in the United States of America.*
FDA Label Image

Numotizine8 (Numotizine8)

Numotizine8 (Numotizine8)
This is a Drug Facts label for Numotizine, a topical analgesic ointment. The active ingredient is Menthol, and it provides temporary relief of muscle pain, soreness, and stiffness for strains, sprains, ligament and tendon injuries, and arthritis. The product should only be used as directed and should be kept out of reach of children. If irritation occurs, usage should stop, and a doctor should be consulted. The jar should be kept sealed and free of any liquid at the top. The inactive ingredients include Clay, Color, Fragrance of Guaiacol, Methyl Guaiacol, and Oil of Wintergreen, Polyols. The label includes contact information for the manufacturer, Hobart Laboratories, Inc., and their website.*
FDA Label Image

Numotizinecarton (Numotizinecarton)

Numotizinecarton (Numotizinecarton)
This is an ointment called NUMOTIZINE which provides temporary relief of pain and soreness. It should only be used externally and not on broken skin or large areas of the body. Contact with eyes and mucous membranes should be avoided. The product is manufactured in the USA by Hobart Laboratories, and the package contains 8 oz (228 grams) of the ointment. The NDC code is 10548-100-08.*
FDA Label Image

Numotizinecartona (Numotizinecartona)

Numotizinecartona (Numotizinecartona)
This is an ointment called ANIWINIO, which seems to contain menthol as a topical analgesic ingredient. The ointment can provide temporary relief of sore muscles, stiffness, sprains, and arthritis. The directions indicate to apply a layer of the ointment on the skin and cover it with a bandage. There are inactive ingredients such as clay, color, fragrance of guaiacol, oil of wintergreen, and polyols. If there are any concerns or questions, users should contact a doctor. It is important to keep the ointment out of the reach of children.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.