1. Home
  2. Labeler Index
  3. Nest Fragrances Llc
  4. NDC Product Code: 72556-002 Nest Fragrances Ginger And Neroli

NDC 72556-002 Nest Fragrances Ginger And Neroli

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72556-002?
  4. Nest Fragrances Ginger And Neroli Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72556-002
Proprietary Name:
Nest Fragrances Ginger And Neroli
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nest Fragrances Llc
Labeler Code:
72556
Product Label ID:
2dfd0edd-7805-4d45-b4fe-82d3173d967d
Start Marketing Date: [9]
12-15-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 72556-002?

The NDC code 72556-002 is assigned by the FDA to the product Nest Fragrances Ginger And Neroli which is product labeled by Nest Fragrances Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72556-002-01 1 tube in 1 carton / 3.2 g in 1 tube. 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 Nest Fragrances Ginger And Neroli?

For sunscreen useApply liberally 15 minutes before sun exposure.Use a water-resistant sunscreen if swimming or sweating.Re-apply at least every 2 hours.Children under 6 months: Ask a doctor.

Which are Nest Fragrances Ginger And Neroli UNII Codes?

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

Which are Nest Fragrances Ginger And Neroli 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".