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  4. NDC Product Code: 78483-001 Holoi

NDC 78483-001 Holoi

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78483-001?
  4. Holoi 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:
78483-001
Proprietary Name:
Holoi
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lifen1 Llc
Labeler Code:
78483
Product Label ID:
75ad61d7-1370-46c7-9018-2f1ec1dfafe1
Start Marketing Date: [9]
06-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78483-001-01

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 78483-001-02

Package Description: 59 mL in 1 BOTTLE, PLASTIC

NDC Code 78483-001-03

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 78483-001-04

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 78483-001?

The NDC code 78483-001 is assigned by the FDA to the product Holoi which is product labeled by Lifen1 Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 78483-001-01 30 ml in 1 bottle, plastic , 78483-001-02 59 ml in 1 bottle, plastic , 78483-001-03 118 ml in 1 bottle, plastic , 78483-001-04 473 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 Holoi?

Spray as much into your pals and thoroughly spread on both hands. Rub into skin until dry.Other informationStore at 20 degrees Celsius (66-77 degrees Fahrenheit).May discolor fabrics.

Which are Holoi UNII Codes?

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

Which are Holoi 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".