Cellamo Phytoboosting Tonic
NDC 77818-305

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 77818-305?
  4. Cellamo Phytoboosting Tonic 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.

Cellamo Phytoboosting Tonic is a UNAPPROVED DRUG OTHER-approved product labeled by Cleanpeace Co., Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 77818-305 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
77818-305
Proprietary Name:
Cellamo Phytoboosting Tonic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Cleanpeace Co., Ltd
Labeler Code:
77818
Product Label ID:
b0e610d3-66f8-ce11-e053-2a95a90a6d49
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
09-08-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 77818-305?

The NDC code 77818-305 is assigned by the FDA to the product Cellamo Phytoboosting Tonic. This pharmaceutical product is labeled by Cleanpeace Co., Ltd and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 77818-305-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Once a day or several times a day, spread evenly on the weak scalp and pat gently for absorption. (Do not rinse and dry naturally )

Which are the associated UNII Codes?

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

  • ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB)
  • ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB) (Active Moiety)
  • HORDEUM VULGARE WHOLE (UNII: 8JBE478M5Q)
  • HORDEUM VULGARE WHOLE (UNII: 8JBE478M5Q) (Active Moiety)
  • LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
  • LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) (Active Moiety)
  • VITEX TRIFOLIA FRUIT (UNII: Q04E1F5351)
  • VITEX TRIFOLIA FRUIT (UNII: Q04E1F5351) (Active Moiety)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
  • RAPHANUS SATIVUS VAR. SATIVUS SEED (UNII: A94I086Q5E)
  • RAPHANUS SATIVUS VAR. SATIVUS SEED (UNII: A94I086Q5E) (Active Moiety)
  • CHINESE CINNAMON (UNII: WS4CQ062KM)
  • CHINESE CINNAMON (UNII: WS4CQ062KM) (Active Moiety)
  • ARCTIUM LAPPA FRUIT (UNII: EA541308MV)
  • ARCTIUM LAPPA FRUIT (UNII: EA541308MV) (Active Moiety)

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".