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  5. NDC Package Code: 83027-0048-1 Industriox

NDC Package 83027-0048-1 Industriox

Berberis Vulgaris,Taraxacum Officinale,Ammonium Carbonicum,Camphora,Spinacia,Sulphuricum - 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:
83027-0048-1
Package Description:
60 mL in 1 BOTTLE, SPRAY
Product Code:
83027-0048
Proprietary Name:
Industriox
Non-Proprietary Name:
Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum, Camphora, Spinacia, Sulphuricum Acidum, Nux Vomica, Acetone, Benzinum, Butyl Methacrylate, Calcarea Carbonica, Lachesis Mutus, Methyl Ethyl Ketone, Naphthalinum, Plumbum Metallicum, Trichloroethylene, Forlmalinum, Mtbe (tert-butyl Methyl Ether), Petroleum, Carboneum Chloratum
Substance Name:
Acetone; Ammonium Carbonate; Benzene; Berberis Vulgaris Root Bark; Camphor (natural); Carbon Tetrachloride; Formaldehyde Solution; Kerosene; Lachesis Muta Venom; Lead; Methyl Ethyl Ketone; N-butyl Methacrylate; Naphthalene; Oyster Shell Calcium Carbonate, Crude; Spinacia Oleracea Root; Strychnos Nux-vomica Seed; Sulfuric Acid; Taraxacum Officinale; Tert-butyl Methyl Ether; Trichloroethylene
Usage Information:
Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. For highly sensitive individuals: best tolerated administration is through imbrication (RUBBING IN) on skin at pulse points or abdomen. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
83027004801
Product Type:
Human Otc Drug
Labeler Name:
Nutritional Specialties, Inc.
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACETONE 12 [hp_X]/mL
  • AMMONIUM CARBONATE 6 [hp_X]/mL
  • BENZENE 12 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • CAMPHOR (NATURAL) 6 [hp_X]/mL
  • CARBON TETRACHLORIDE 20 [hp_X]/mL
  • FORMALDEHYDE SOLUTION 12 [hp_X]/mL
  • KEROSENE 16 [hp_X]/mL
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • LEAD 12 [hp_X]/mL
  • METHYL ETHYL KETONE 12 [hp_X]/mL
  • N-BUTYL METHACRYLATE 12 [hp_X]/mL
  • NAPHTHALENE 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • SPINACIA OLERACEA ROOT 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 8 [hp_X]/mL
  • SULFURIC ACID 6 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • TERT-BUTYL METHYL ETHER 16 [hp_X]/mL
  • TRICHLOROETHYLENE 12 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-25-2023
    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 83027-0048-1?

    The NDC Packaged Code 83027-0048-1 is assigned to a package of 60 ml in 1 bottle, spray of Industriox, a human over the counter drug labeled by Nutritional Specialties, Inc.. The product's dosage form is spray and is administered via oral form.

    Is NDC 83027-0048 included in the NDC Directory?

    Yes, Industriox with product code 83027-0048 is active and included in the NDC Directory. The product was first marketed by Nutritional Specialties, Inc. on September 25, 2023 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 83027-0048-1?

    The 11-digit format is 83027004801. 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 5-4-1 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
    5-4-183027-0048-15-4-283027-0048-01