NDC 72312-0020 Absolute Ppc

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:
72312-0020
Proprietary Name:
Absolute Ppc
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
72312
Start Marketing Date: [9]
10-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 72312-0020?

The NDC code 72312-0020 is assigned by the FDA to the product Absolute Ppc which is product labeled by Cellalab. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72312-0020-1 250 ml in 1 jar . 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 Absolute Ppc?

1. Apply PPC magic Cream on the body parts (abdomen, thigh, arms) where you want slimming. Massage the area either with your hand or roller for 10~20 minutes. 2. Apply PPC magic cream one more time and wrap the area with a plastic wrap. 3. Wait for 30 minutes for better absorption. Then, remove the wrap and wipe the cream off. (maintain the wrapping for 30min.~1hour depending on individual condition)4. Due to the ingredients for efficacy, the skin may be red when removing the wrap. If it returns to normal skin color after 10 minutes, it is not an adverse reaction. 5. It is recommended to use in small areas for the first time to see if it is suitable for your skin.

Which are Absolute Ppc UNII Codes?

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

Which are Absolute Ppc 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".