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NDC 83665-001 Balance

Adrenalinum,Adrenocorticotrophin (30x,100x),Agrimonia Eup Flos,Anacardium,Antimon - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83665-001?
  4. Balance Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
83665-001
Proprietary Name:
Balance
Non-Proprietary Name: [1]
Adrenalinum, Adrenocorticotrophin (30x, 100x), Agrimonia Eup Flos, Anacardium, Antimon Crud, Calc Carb, Castanea Sativa Flos, Cortisone Aceticum, Fucus, Hypothalamus, Kali Bic, Oleander, Pituitarum Popsterium, Sabadilla, Staphysag, Thyroidinum
Substance Name: [2]
Agrimonia Eupatoria Flower; Antimony Trisulfide; Bos Taurus Hypothalamus; Castanea Sativa Flower; Corticotropin; Cortisone Acetate; Delphinium Staphisagria Seed; Epinephrine; Fucus Vesiculosus; Nerium Oleander Leaf; Oyster Shell Calcium Carbonate, Crude; Potassium Dichromate; Schoenocaulon Officinale Seed; Semecarpus Anacardium Juice; Sus Scrofa Pituitary Gland, Posterior; Thyroid, Unspecified
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]
    Eatactics, Llc
    Labeler Code:
    83665
    Product Label ID:
    05c08c20-15bf-b095-e063-6294a90a3029
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-19-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 83665-001?

    The NDC code 83665-001 is assigned by the FDA to the product Balance which is a human over the counter drug product labeled by Eatactics, Llc. The generic name of Balance is adrenalinum, adrenocorticotrophin (30x, 100x), agrimonia eup flos, anacardium, antimon crud, calc carb, castanea sativa flos, cortisone aceticum, fucus, hypothalamus, kali bic, oleander, pituitarum popsterium, sabadilla, staphysag, thyroidinum. 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 83665-001-01 59 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 Balance?

    Initially, depress pump until primed.Spray one dose directly into mouth.Adults 12 & up: 3 sprays 3 times per day. Consult a physician for use in children under 12 years of age.Use addtiionally as needed, up to 6 times per day.

    What are Balance 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 Balance UNII Codes?

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

    • FUCUS VESICULOSUS (UNII: 535G2ABX9M)
    • FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
    • EPINEPHRINE (UNII: YKH834O4BH)
    • EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
    • CORTICOTROPIN (UNII: K0U68Q2TXA)
    • CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
    • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
    • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
    • CORTISONE ACETATE (UNII: 883WKN7W8X)
    • CORTISONE (UNII: V27W9254FZ) (Active Moiety)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
    • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
    • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
    • SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T)
    • SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (Active Moiety)
    • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
    • THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
    • ANTIMONY TRISULFIDE (UNII: F79059A38U)
    • ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
    • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7)
    • BOS TAURUS HYPOTHALAMUS (UNII: S6G2NLH4Y7) (Active Moiety)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
    • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
    • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
    • POTASSIUM DICHROMATE (UNII: T4423S18FM)
    • DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
    • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
    • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
    • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)

    Which are Balance 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:

    Which are the Pharmacologic Classes for Balance?

    * 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".