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NDC 49215-0006 Test Flex

Avena Sativa,Calcarea Carbonica,Damiana,Glandula Suprarenalis Suis,Hypophysis - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49215-0006?
  4. Test Flex Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
49215-0006
Proprietary Name:
Test Flex
Non-Proprietary Name: [1]
Avena Sativa, Calcarea Carbonica, Damiana, Glandula Suprarenalis Suis, Hypophysis Suis, Magnesia Carbonica, Millefolium, Sabal Serrulata, Thuja Occidentalis, Urtica Urens
Substance Name: [2]
Achillea Millefolium; Avena Sativa Flowering Top; Magnesium Carbonate; Oyster Shell Calcium Carbonate, Crude; Saw Palmetto; Sus Scrofa Adrenal Gland; Sus Scrofa Pituitary Gland; Thuja Occidentalis Leaf; Turnera Diffusa Leafy Twig; Urtica Urens
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Safe Anabolic Sciences
    Labeler Code:
    49215
    Product Label ID:
    fed38357-f3b7-42f0-9367-eaf97e15c059
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-17-2017
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 49215-0006?

    The NDC code 49215-0006 is assigned by the FDA to the product Test Flex which is a human over the counter drug product labeled by Safe Anabolic Sciences. The generic name of Test Flex is avena sativa, calcarea carbonica, damiana, glandula suprarenalis suis, hypophysis suis, magnesia carbonica, millefolium, sabal serrulata, thuja occidentalis, urtica urens. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 49215-0006-1 30 ml in 1 bottle, spray . 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 Test Flex?

    Adults only, spray twice under the tongue, three times a day.

    What are Test Flex 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 Test Flex UNII Codes?

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

    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
    • TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
    • TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
    • SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
    • SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
    • SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
    • SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
    • MAGNESIUM CARBONATE (UNII: 0E53J927NA)
    • CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
    • SAW PALMETTO (UNII: J7WWH9M8QS)
    • SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
    • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
    • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
    • URTICA URENS (UNII: IHN2NQ5OF9)
    • URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)

    Which are Test Flex 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.

    [11] 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.

    [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".