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NDC 70327-0002 Natural Fit

Kali Phosphoricum,Natrum Sulphuricum,Agnus Castus,Chelidonium Majus,Fucus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70327-0002?
  4. Natural Fit Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
70327-0002
Proprietary Name:
Natural Fit
Non-Proprietary Name: [1]
Kali Phosphoricum, Natrum Sulphuricum, Agnus Castus, Chelidonium Majus, Fucus Vesiculosus, Lycopodium Clavatum, Thuja Occidentalis, Capsicum Annuum, Carduus Marianus, Cysteinum, Hydrocotyle Asiatica, Kali Carbonicum, Nux Vomica, Phytolacca Decandra, Rosa Canina, Flos, Salix Alba, Thea Sinensis, Gambogia, Carbo Vegetabilis, Calcarea Carbonica, Graphites, Natrum Muriaticum, Natrum Phosphoricum, Glandula Suprarenalis Suis, Hepar Suis, Pancreas Suis, Pituitarum Posterium (bovine), Placenta Totalis Suis,
Substance Name: [2]
Activated Charcoal; Bos Taurus Pituitary Gland, Posterior; Capsicum; Centella Asiatica Whole; Chaste Tree Fruit; Chelidonium Majus Whole; Cysteine; Dibasic Potassium Phosphate; Fucus Vesiculosus; Gamboge; Graphite; Green Tea Leaf; Gymnema Sylvestre Leaf; Lycopodium Clavatum Spore; Milk Thistle; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Pork Liver; Potassium Carbonate; Rosa Canina Flower; Salix Alba Bark; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Strychnos Nux-vomica Seed; Sus Scrofa Adrenal Gland; Sus Scrofa Pancreas; Sus Scrofa Placenta; Thuja Occidentalis Leafy Twig; Thyroid, Bovine; Water
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Advanced Healthcare Solutions
    Labeler Code:
    70327
    Product Label ID:
    6b480f87-18b4-444b-8905-5fb046135688
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-18-2020
    End Marketing Date: [10]
    09-18-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 70327-0002?

    The NDC code 70327-0002 is assigned by the FDA to the product Natural Fit which is a human over the counter drug product labeled by Advanced Healthcare Solutions. The generic name of Natural Fit is kali phosphoricum, natrum sulphuricum, agnus castus, chelidonium majus, fucus vesiculosus, lycopodium clavatum, thuja occidentalis, capsicum annuum, carduus marianus, cysteinum, hydrocotyle asiatica, kali carbonicum, nux vomica, phytolacca decandra, rosa canina, flos, salix alba, thea sinensis, gambogia, carbo vegetabilis, calcarea carbonica, graphites, natrum muriaticum, natrum phosphoricum, glandula suprarenalis suis, hepar suis, pancreas suis, pituitarum posterium (bovine), placenta totalis suis, . The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 70327-0002-1 60 ml in 1 bottle, dropper . 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 Natural Fit?

    Supports metabolism. Supports metabolism.

    What are Natural Fit Active Ingredients?

    An 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.

    Which are Natural Fit UNII Codes?

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

    Which are Natural Fit 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

    [1] 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.

    [2] What is the Substance Name? - An 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [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.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [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".