NDC 76642-010 Yan Plus Super Medic

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:
76642-010
Proprietary Name:
Yan Plus Super Medic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tripeople Cosmetic Co.,ltd.
Labeler Code:
76642
Start Marketing Date: [9]
05-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76642-010-01

Package Description: 200 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 76642-010?

The NDC code 76642-010 is assigned by the FDA to the product Yan Plus Super Medic which is product labeled by Tripeople Cosmetic Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76642-010-01 200 ml in 1 bottle, spray . 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 Yan Plus Super Medic?

Directions• Spray this evenly on the surface of the skin or the object, or rub it on the surface 2times. Will dry out soon.

Which are Yan Plus Super Medic UNII Codes?

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

Which are Yan Plus Super Medic 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".