NDC 70945-100 Tolcylen Antifungal Solution

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70945-100
Proprietary Name:
Tolcylen Antifungal Solution
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70945
Start Marketing Date: [9]
12-16-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - CLEAR FLUID)

Code Structure Chart

Product Details

What is NDC 70945-100?

The NDC code 70945-100 is assigned by the FDA to the product Tolcylen Antifungal Solution which is product labeled by Marlinz Pharma, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70945-100-75 1 tube, with applicator in 1 carton / 7.5 ml in 1 tube, with applicator. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Tolcylen Antifungal Solution?

Wash the affected area with soap and water.■ Dry thoroughly, then apply a thin layer over the affected area.■ Use twice daily (morning and night) or as directed by a physician.■ Pay special attention to the spaces between the toes and the areas around the edges and under the front of the nails.■ Wear well-fitted ventilated shoes and change socks at least once daily.■ Use daily for four (4) weeks. If condition persists longer, consult a physician.■ Wash hands after each use. Store and use at room temperature.

Which are Tolcylen Antifungal Solution UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Tolcylen Antifungal Solution Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Tolcylen Antifungal Solution?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Patient Education

Tolnaftate


Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".