NDC 43853-0014 Dna Rna

Arnica Montana,Avena Sativa,Damiana,Dna,Hypophysis Suis,Oleum Animale,Panax - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43853-0014
Proprietary Name:
Dna Rna
Non-Proprietary Name: [1]
Arnica Montana, Avena Sativa, Damiana, Dna, Hypophysis Suis, Oleum Animale, Panax Ginseng, Rna, Thuja Occidentalis
Substance Name: [2]
Arnica Montana; Asian Ginseng; Avena Sativa Flowering Top; Cervus Elaphus Horn Oil; Herring Sperm Dna; Saccharomyces Cerevisiae Rna; Sus Scrofa Pituitary Gland; Thuja Occidentalis Leafy Twig; Turnera Diffusa Leafy Twig
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]
    Problen
    Labeler Code:
    43853
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    11-23-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43853-0014-1

    Package Description: 30 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 43853-0014?

    The NDC code 43853-0014 is assigned by the FDA to the product Dna Rna which is a human over the counter drug product labeled by Problen. The generic name of Dna Rna is arnica montana, avena sativa, damiana, dna, hypophysis suis, oleum animale, panax ginseng, rna, thuja occidentalis. 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 43853-0014-1 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 Dna Rna?

    Temporarily supports symptoms of a run-down condition or advancing age. Symptoms may include: Low energy, poor muscular strength and stamina, pain and stiffness in muscles and joints, forgetfulness, inability to concentrate. Temporarily supports symptoms of a run-down condition or advancing age. Symptoms may include: Low energy, poor muscular strength and stamina, pain and stiffness in muscles and joints, forgetfulness, inability to concentrate.

    What are Dna Rna 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 Dna Rna UNII Codes?

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

    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
    • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
    • TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
    • TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
    • HERRING SPERM DNA (UNII: 51FI676N6F)
    • HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)
    • SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
    • SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
    • CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12)
    • CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12) (Active Moiety)
    • ASIAN GINSENG (UNII: CUQ3A77YXI)
    • ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
    • SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
    • SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)

    Which are Dna Rna 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".