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  4. NDC Product Code: 69684-320 Hairfill Scalp Hair Essential

NDC 69684-320 Hairfill Scalp Hair Essential

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69684-320?
  4. Hairfill Scalp Hair Essential 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:
69684-320
Proprietary Name:
Hairfill Scalp Hair Essential
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Secretipss Co., Ltd.
Labeler Code:
69684
Product Label ID:
9bf32587-5547-4450-8d5e-c2c8db2cca0a
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69684-320-01

Package Description: 240 mL in 1 BOTTLE

Product Details

What is NDC 69684-320?

The NDC code 69684-320 is assigned by the FDA to the product Hairfill Scalp Hair Essential which is product labeled by Secretipss Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69684-320-01 240 ml in 1 bottle . 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 Hairfill Scalp Hair Essential?

Direction & Dosage: After throughly wetting the hair and scalp with lukewarm water, evenly massage the scalp with 3-5 ml of the product. Leave it on for 3 minutes and then wash off.

Which are Hairfill Scalp Hair Essential UNII Codes?

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

Which are Hairfill Scalp Hair Essential 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".