NDC 81823-010 Anacell

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:
81823-010
Proprietary Name:
Anacell
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
D-nature Co., Ltd.
Labeler Code:
81823
Start Marketing Date: [9]
06-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81823-010-02

Package Description: 30 CONTAINER in 1 CARTON / 1 mL in 1 CONTAINER (81823-010-01)

Product Details

What is NDC 81823-010?

The NDC code 81823-010 is assigned by the FDA to the product Anacell which is product labeled by D-nature Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81823-010-02 30 container in 1 carton / 1 ml in 1 container (81823-010-01). 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 Anacell?

After shampooing hair, dry it well and shaking the product sufficiently, apply an appropriate amount evenly to the scalp and rub it to absorb enough.The best usage time is 3 to 8 hours.Do not use for more than 8 hours.Wash off with shampoo after use.**Use the electric vibration hair massage device to maximize results. (5 to 10 minutes)**

Which are Anacell UNII Codes?

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

  • CENTIPEDA MINIMA WHOLE (UNII: 7F196Q97IQ)
  • CENTIPEDA MINIMA WHOLE (UNII: 7F196Q97IQ) (Active Moiety)

Which are Anacell 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".