NDC 69958-130 Cre Am2ate Knight Seahorse

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:
69958-130
Proprietary Name:
Cre Am2ate Knight Seahorse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
J2d International
Labeler Code:
69958
Start Marketing Date: [9]
09-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69958-130-02

Package Description: 1 CONTAINER in 1 CARTON / 50 mL in 1 CONTAINER (69958-130-01)

Product Details

What is NDC 69958-130?

The NDC code 69958-130 is assigned by the FDA to the product Cre Am2ate Knight Seahorse which is product labeled by J2d International. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69958-130-02 1 container in 1 carton / 50 ml in 1 container (69958-130-01). 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 Cre Am2ate Knight Seahorse?

Directions: 1.Take an adequate amount onto your palms after applying toner in the morning and evening, 2.and evenly spread onto the face and neck.

Which are Cre Am2ate Knight Seahorse UNII Codes?

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

Which are Cre Am2ate Knight Seahorse 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".