81812-0101 NDC - HAIR AF (BETULA PUBESCENS FLOWER BUD, CASTANEA SATIVA LEAF, HUMAN HAIR, PHOSPHORUS, POPULUS NIGRA LEAF BUD, AND SACCHAROMYCES CEREVISIAE RNA)

Drug Information

Product NDC: 81812-0101

Proprietary Name: Hair AF

Non Proprietary Name: betula pubescens flower bud, castanea sativa leaf, human hair, phosphorus, populus nigra leaf bud, and saccharomyces cerevisiae rna

Active Ingredient(s):
  • 2 [hp_X]/mL BETULA PUBESCENS FLOWER BUD;
  • 2 [hp_X]/mL CASTANEA SATIVA LEAF;
  • 7 [hp_X]/mL HUMAN HAIR;
  • 7 [hp_X]/mL PHOSPHORUS;
  • 2 [hp_X]/mL POPULUS NIGRA LEAF BUD;
  • 4 [hp_X]/mL SACCHAROMYCES CEREVISIAE RNA


Administration Route(s): SUBLINGUAL

Dosage Form(s): SOLUTION

Labeler Information

Labeler Name: GC Love LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/1/2021

Package Information

No. Package Code Package Description Billing Unit
181812-0101-160 mL in 1 BOTTLE, GLASS (81812-0101-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC81812-0101The 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 NAMEHair AFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEbetula pubescens flower bud, castanea sativa leaf, human hair, phosphorus, populus nigra leaf bud, and saccharomyces cerevisiae rnaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEGC Love LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBETULA PUBESCENS FLOWER BUD; CASTANEA SATIVA LEAF; HUMAN HAIR; PHOSPHORUS; POPULUS NIGRA LEAF BUD; SACCHAROMYCES CEREVISIAE RNAAn 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 STRENGTH2; 2; 7; 7; 2; 4 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

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This page was last updated on: 2/1/2023