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  5. NDC Package Code: 17089-350-18 Guna-awareness

NDC Package 17089-350-18 Guna-awareness

Betaine - Bufo Bufo Cutaneous Gland - Calcium Carbonate - Chromic Sulfate - Cicuta Virosa - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17089-350-18
Package Description:
1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Code:
17089-350
Proprietary Name:
Guna-awareness
Non-Proprietary Name:
Betaine - Bufo Bufo Cutaneous Gland - Calcium Carbonate - Chromic Sulfate - Cicuta Virosa Root - Copper - Folic Acid - Gold - Cobalamin - Iron - Lachesis Muta Venom - Melatonin - Molybdenum - Neurotrophin-3 - Neurotrophin-4 - Oxytocin - Silicon Dioxide - Sus Scrofa Frontal Lobe - Sus Scrofa Temporal Lobe - Thyrotropin Alfa - Ubidecarenone - Vanadium - Zinc - Brain-derived Neurotrophic Factor Human -
Substance Name:
Betaine; Brain-derived Neurotrophic Factor Human; Bufo Bufo Cutaneous Gland; Calcium Carbonate; Chromic Sulfate; Cicuta Virosa Root; Cobalamin; Copper; Folic Acid; Gold; Iron; Lachesis Muta Venom; Melatonin; Molybdenum; Neurotrophin-3; Neurotrophin-4; Oxytocin; Silicon Dioxide; Sus Scrofa Frontal Lobe; Sus Scrofa Temporal Lobe; Thyrotropin Alfa; Ubidecarenone; Vanadium; Zinc
Usage Information:
Take 15 minutes before mealsAdults and children 12 years and older    20 drops in a little water, 2 times per dayChildren  between 12 years and 6 years of age    10 drops in a little water, 2 times per dayChildren under 6 years     5 drops in a glass of water, 2 times per day
11-Digit NDC Billing Format:
17089035018
Product Type:
Human Otc Drug
Labeler Name:
Guna Spa
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BETAINE 3 [hp_X]/30mL
  • BRAIN-DERIVED NEUROTROPHIC FACTOR HUMAN 4 [hp_C]/30mL
  • BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/30mL
  • CALCIUM CARBONATE 3 [hp_X]/30mL
  • CHROMIC SULFATE 3 [hp_X]/30mL
  • CICUTA VIROSA ROOT 12 [hp_X]/30mL
  • COBALAMIN 3 [hp_X]/30mL
  • COPPER 12 [hp_X]/30mL
  • FOLIC ACID 3 [hp_X]/30mL
  • GOLD 12 [hp_X]/30mL
  • IRON 3 [hp_X]/30mL
  • LACHESIS MUTA VENOM 12 [hp_X]/30mL
  • MELATONIN 4 [hp_C]/30mL
  • MOLYBDENUM 3 [hp_X]/30mL
  • NEUROTROPHIN-3 4 [hp_C]/30mL
  • NEUROTROPHIN-4 4 [hp_C]/30mL
  • OXYTOCIN 6 [hp_X]/30mL
  • SILICON DIOXIDE 12 [hp_X]/30mL
  • SUS SCROFA FRONTAL LOBE 6 [hp_X]/30mL
  • SUS SCROFA TEMPORAL LOBE 6 [hp_X]/30mL
  • THYROTROPIN ALFA 3 [hp_X]/30mL
  • UBIDECARENONE 3 [hp_X]/30mL
  • VANADIUM 6 [hp_X]/30mL
  • ZINC 3 [hp_X]/30mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Uterine Smooth Muscle Contraction or Tone - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Methylating Activity - [MoA] (Mechanism of Action)
  • Methylating Agent - [EPC] (Established Pharmacologic Class)
  • Oxytocic - [EPC] (Established Pharmacologic Class)
  • Oxytocin - [CS]
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Thyroid Stimulating Hormone - [EPC] (Established Pharmacologic Class)
  • Thyrotropin - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    04-16-2008
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17089-350-18?

    The NDC Packaged Code 17089-350-18 is assigned to a package of 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper of Guna-awareness, a human over the counter drug labeled by Guna Spa. The product's dosage form is solution/ drops and is administered via oral form.

    Is NDC 17089-350 included in the NDC Directory?

    Yes, Guna-awareness with product code 17089-350 is active and included in the NDC Directory. The product was first marketed by Guna Spa on April 16, 2008 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17089-350-18?

    The 11-digit format is 17089035018. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-217089-350-185-4-217089-0350-18