NDC 70908-090 Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet

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:
70908-090
Proprietary Name:
Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70908
Start Marketing Date: [9]
02-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 70908-090?

The NDC code 70908-090 is assigned by the FDA to the product Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet which is product labeled by Mefactory Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70908-090-01 .2 g in 1 pouch . 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 Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet?

Indications & Usage: Wet your nose with warm water and place step2 with dry hands. Let dry for 10minutes until stiff to the touch and slowly and carefully peel off starting at deges, pulling toward center. For the best result, be sure to remove strip as directed promptly after it becomes stiff and do not get it wet again.

Which are Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet UNII Codes?

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

Which are Mefactory 3step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet 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:

* 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".