NDC 81812-0101 Hair Af

Betula Pubescens Flower Bud, Castanea Sativa Leaf, Human Hair, Phosphorus, Populus Nigra Leaf Bud, And Saccharomyces Cerevisiae Rna

NDC Product Code 81812-0101

NDC CODE: 81812-0101

Proprietary Name: Hair Af What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Betula Pubescens Flower Bud, Castanea Sativa Leaf, Human Hair, Phosphorus, Populus Nigra Leaf Bud, And Saccharomyces Cerevisiae Rna What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 81812-0101-1

Package Description: 60 mL in 1 BOTTLE, GLASS

NDC Product Information

Hair Af with NDC 81812-0101 is a a human over the counter drug product labeled by Gc Love Llc. The generic name of Hair Af is betula pubescens flower bud, castanea sativa leaf, human hair, phosphorus, populus nigra leaf bud, and saccharomyces cerevisiae rna. The product's dosage form is solution and is administered via sublingual form.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Hair Af Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Sublingual - Administration beneath the tongue.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Gc Love Llc
Labeler Code: 81812
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 11-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Hair Af Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts

Distributed by GC Love, LLC.

Otc - Active Ingredient

Active IngredientsBetula Pubescens Flower Bud2XCastanea Vesca2XHuman Hair4C 7CPhosphorus5X 6X 8X 12X 3C 5C 6C 7CPopulus Nigra Leaf Bud2XRNA3x 4x

Otc - Purpose

  • For temporary relief of minor:hair lossClaims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.itchy scalpscaliness of scalp

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use. Do not use if clear seal over the cap is broken or missing.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Otc - Stop Use

Stop use and ask a doctor if hair loss, itchy scalp, scaliness of scalp, or other symptoms do not improve within 7 days or are accompanied by fever.

Directions

Adults: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional.

Inactive Ingredients

Alcohol (20% by volume), distilled water

Questions?

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* Please review the disclaimer below.