NDC 53093-433 Motto

NDC Product Code 53093-433

NDC 53093-433-47

Package Description: 2 PATCH in 1 PACKAGE > 9 mg in 1 PATCH

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Motto with NDC 53093-433 is a product labeled by Motto-elektro Ltd.. The generic name of Motto is . The product's dosage form is and is administered via form.

Labeler Name: Motto-elektro Ltd.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.


Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Motto-elektro Ltd.
Labeler Code: 53093
Start Marketing Date: 03-10-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Motto Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index


  • External analgesicUsesReleives chronic and acute pain of muscles and joints due to:rheumatic complaintslumbagoheadachetennis elbowmenstrual pain

Active Ingredient

Sulfur 9 mg


  • For external use onlyIf pregnant or breast-feeding, ask a health professional before useAllergy alert:This product contains natural rubber latex which may cause allergic reactions.Do not useon woundson irritated or damaged skinwith a heating padotherwise than as directedStop use and ask a doctor ifexcessive irritation of the skin developscondition worsensskin rush occurs

Keep Out Of Reach Of Children

To avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away.


Clean the affected area. Remove the silikon paper film from the patch.


  • Adults and children 12 years of age and older: cut up a patch into pieces of desired sizes and apply to affected area. Use up to 10 days.children under 12 years of age: do not use, consult your physicianuse according to the User Guide inside the packagerefer to the above warnings; use otherwise than as directed may be dangerousOther informationStore at room temperature 15° to 30°C (59° to 86°F), away from sunlight.

Inactive Ingredient

Zinc oxide, on an adhesive bandage backing with a protective paper

* Please review the disclaimer below.