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  4. NDC Product Code: 29500-9317 Hootin Pomegranate

NDC 29500-9317 Hootin Pomegranate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 29500-9317?
  4. Hootin Pomegranate 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:
29500-9317
Proprietary Name:
Hootin Pomegranate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Personal Care Products Llc
Labeler Code:
29500
Product Label ID:
069951e5-c32c-47f9-ac05-73c916b89f91
Start Marketing Date: [9]
09-21-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 29500-9317-1

Package Description: 30 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 29500-9317?

The NDC code 29500-9317 is assigned by the FDA to the product Hootin Pomegranate which is product labeled by Personal Care Products Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 29500-9317-1 30 ml in 1 bottle, plastic . 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 Hootin Pomegranate?

Wet hands thoroughly with product and rub into skin until dry.Children under 6 years of age should be supervised by an adult when using.

Which are Hootin Pomegranate UNII Codes?

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

Which are Hootin Pomegranate 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".