NDC 53113-263 Gadaderm Antifungal
NDC Product Code 53113-263
Proprietary Name: Gadaderm Antifungal What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 53113 - Gadal Laboratories Inc
- 53113-263 - Gadaderm Antifungal
NDC 53113-263-01
Package Description: 1 TUBE in 1 BOX > 28 g in 1 TUBE
NDC Product Information
Gadaderm Antifungal with NDC 53113-263 is a product labeled by Gadal Laboratories Inc. The generic name of Gadaderm Antifungal is . The product's dosage form is and is administered via form.
Labeler Name: Gadal Laboratories Inc
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.
- MINERAL OIL (UNII: T5L8T28FGP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- WATER (UNII: 059QF0KO0R)
- CETEARETH-6 (UNII: 2RJS3559D3)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Gadal Laboratories Inc
Labeler Code: 53113
Start Marketing Date: 01-01-2013 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’.
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Information for Patients
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