1. Home
  2. Labeler Index
  3. Rite Aid
  4. NDC Product Code: 11822-9650 Rite Aid Maximum Strength Foot Care Anti-fungal Pen

NDC 11822-9650 Rite Aid Maximum Strength Foot Care Anti-fungal Pen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11822-9650?
  4. Rite Aid Maximum Strength Foot Care Anti-fungal Pen Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11822-9650
Proprietary Name:
Rite Aid Maximum Strength Foot Care Anti-fungal Pen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid
Labeler Code:
11822
Product Label ID:
a3f907ab-f6e6-422d-8a5e-0aa6118d0da2
Start Marketing Date: [9]
12-10-2013
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 11822-9650?

The NDC code 11822-9650 is assigned by the FDA to the product Rite Aid Maximum Strength Foot Care Anti-fungal Pen which is product labeled by Rite Aid. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-9650-2 1 applicator in 1 box / 1.7 ml in 1 applicator (11822-9650-1). 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 Rite Aid Maximum Strength Foot Care Anti-fungal Pen?

Read all warnings and directionsuse only as directedclean the affected area with soap and water and dry thoroughlyremove cap from pentwist the base of the pen, with brush pointing downward, until product dispensesapply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctorfor athlete’s foot, pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete’s foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctorintended for use by normally healthy adults onlypersons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctorsupervise children in the use of this productthis product is not effective on the scalp or nails

Which are Rite Aid Maximum Strength Foot Care Anti-fungal Pen UNII Codes?

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

Which are Rite Aid Maximum Strength Foot Care Anti-fungal Pen 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 Rite Aid Maximum Strength Foot Care Anti-fungal Pen?

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:

* Please review the disclaimer below.

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".