NDC 69264-016 Callus Removal Foot Pack

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:
69264-016
Proprietary Name:
Callus Removal Foot Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Polaroisin International Co., Ltd.
Labeler Code:
69264
Start Marketing Date: [9]
12-17-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69264-016-25

Package Description: 2 PATCH in 1 BAG

Product Details

What is NDC 69264-016?

The NDC code 69264-016 is assigned by the FDA to the product Callus Removal Foot Pack which is product labeled by Polaroisin International Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69264-016-25 2 patch in 1 bag . 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 Callus Removal Foot Pack?

Wash your feetTake out the foot mask by cutting along the dotted blue line with scissorWear the foot mask and attach adhesive tape to secure the footPut the feet in the mask for about 60-70 minutesTake off the foot mask and wash away the lotion from the feetSoak feet in warm water for 10 mins(everyday) to accelerate peeling effectsCallus will start exfoliating after 3 days (no rubbing, it will peel off automatically). After 1 week, all calluses will be removed!

Which are Callus Removal Foot Pack UNII Codes?

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

Which are Callus Removal Foot Pack 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:

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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".