NDC 71006-030 Rubelli Wine Foot Packs

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:
71006-030
Proprietary Name:
Rubelli Wine Foot Packs
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rubelli Co.,ltd
Labeler Code:
71006
Start Marketing Date: [9]
09-01-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71006-030-02

Package Description: 4 POUCH in 1 CARTON / 50 g in 1 POUCH (71006-030-01)

Product Details

What is NDC 71006-030?

The NDC code 71006-030 is assigned by the FDA to the product Rubelli Wine Foot Packs which is product labeled by Rubelli Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71006-030-02 4 pouch in 1 carton / 50 g in 1 pouch (71006-030-01). 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 Rubelli Wine Foot Packs?

Directions:1. Open the product and wear the “Foot Pack”. 2. After wearing the “Foot Pack”, wear the vinyl gloves. 3. To fully absorb the essence, evenly massage feet. 4. 30 minutes later, remove the “Foot Pack” and then pat the skin to absorb the left essence. 5. You can maintain smooth and moist skin by repetitively using it 3-4 times a week.

Which are Rubelli Wine Foot Packs UNII Codes?

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

Which are Rubelli Wine Foot Packs 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".