84718-001 NDC - EELHOE HAIR GROWTH (KOHHII EKISU)

Drug Information

  • Product NDC: 84718-001
  • Proprietary Name: EELHOE Hair Growth
  • Non Proprietary Name: KOHHII EKISU
  • Active Ingredient(s): 10 g/1000g ARABICA COFFEE BEAN; 80 g/1000g ARGAN OIL; 600 g/1000g CASTOR OIL; 300 g/1000g COCONUT OIL; 10 g/1000g ROSEMARY OIL
  • Administration Route(s): TOPICAL
  • Dosage Form(s): OIL
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Shenzhen Chuangwei Electronic Technology Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:9/26/2024

Package Information

No. Package Code Package Description Billing Unit
184718-001-011 BOTTLE in 1 BOX (84718-001-01) / 60 g in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC84718-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEEELHOE Hair GrowthThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEKOHHII EKISUThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEOILThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/26/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEShenzhen Chuangwei Electronic Technology Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARABICA COFFEE BEAN; ARGAN OIL; CASTOR OIL; COCONUT OIL; ROSEMARY OILAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 80; 600; 300; 10 
ACTIVE INGRED UNITg/1000g; g/1000g; g/1000g; g/1000g; g/1000g 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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This page was last updated on: 11/21/2025