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  5. NDC Package Code: 69390-001-01 Ear Rx

NDC Package 69390-001-01 Ear Rx

Aconitum Nap,Baryta Carb,Belladonna,Calc Carb,Capsicum,Carbo - 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:
69390-001-01
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
69390-001
Proprietary Name:
Ear Rx
Non-Proprietary Name:
Aconitum Nap, Baryta Carb, Belladonna, Calc Carb, Capsicum, Carbo Veg, Causticum, Chamomilla, Ferrum Phos, Hepar Sulph Calc, Kali Mur, Lachesis, Lycopodium, Mercurius Sol, Natrum Mur, Plantago, Pulsatilla, Silicea, Sulphur, Verbascum
Substance Name:
Aconitum Napellus; Activated Charcoal; Atropa Belladonna; Barium Carbonate; Calcium Sulfide; Capsicum; Causticum; Ferrosoferric Phosphate; Lachesis Muta Venom; Lycopodium Clavatum Spore; Matricaria Recutita; Mercurius Solubilis; Oyster Shell Calcium Carbonate, Crude; Plantago Major; Potassium Chloride; Pulsatilla Vulgaris; Silicon Dioxide; Sodium Chloride; Sulfur; Verbascum Thapsus
Usage Information:
Shake well and take 5 drops under tongue 3 times a day for 10 days. Take at least 15 minutes away from eating or drinking.
11-Digit NDC Billing Format:
69390000101
Product Type:
Human Otc Drug
Labeler Name:
Miami Beach Pediatrics Pa
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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACONITUM NAPELLUS 6 [hp_X]/mL
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • ATROPA BELLADONNA 9 [hp_X]/mL
  • BARIUM CARBONATE 10 [hp_X]/mL
  • CALCIUM SULFIDE 10 [hp_X]/mL
  • CAPSICUM 9 [hp_X]/mL
  • CAUSTICUM 8 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 9 [hp_X]/mL
  • LACHESIS MUTA VENOM 8 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
  • MATRICARIA RECUTITA 9 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_X]/mL
  • PLANTAGO MAJOR 9 [hp_X]/mL
  • POTASSIUM CHLORIDE 10 [hp_X]/mL
  • PULSATILLA VULGARIS 9 [hp_X]/mL
  • SILICON DIOXIDE 9 [hp_X]/mL
  • SODIUM CHLORIDE 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • VERBASCUM THAPSUS 6 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Vegetable Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-23-2015
    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 69390-001-01?

    The NDC Packaged Code 69390-001-01 is assigned to a package of 30 ml in 1 bottle, dropper of Ear Rx, a human over the counter drug labeled by Miami Beach Pediatrics Pa. The product's dosage form is liquid and is administered via oral form.

    Is NDC 69390-001 included in the NDC Directory?

    Yes, Ear Rx with product code 69390-001 is active and included in the NDC Directory. The product was first marketed by Miami Beach Pediatrics Pa on November 23, 2015 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 69390-001-01?

    The 11-digit format is 69390000101. 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
    5-3-269390-001-015-4-269390-0001-01