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  5. NDC Package Code: 62795-1040-2 T-relief Pro Spasm

NDC Package 62795-1040-2 T-relief Pro Spasm

Aconitum Napellus, Amanita Muscaria Fruiting Body,Ammonium Bromide,Atropine Sulfate,Atropa - 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:
62795-1040-2
Package Description:
90 TABLET in 1 BOTTLE
Product Code:
62795-1040
Proprietary Name:
T-relief Pro Spasm
Non-Proprietary Name:
Aconitum Napellus, Amanita Muscaria Fruiting Body, Ammonium Bromide, Atropine Sulfate, Atropa Belladonna, Matricaria Recutita, Citrullus Colocynthis Fruit Pulp, Magnesium Phosphate, Dibasic Trihydrate, Passiflora Incarnata Flowering Top, And Veratrum Album Root
Substance Name:
Aconitum Napellus; Amanita Muscaria Fruiting Body; Ammonium Bromide; Atropa Belladonna; Atropine Sulfate; Citrullus Colocynthis Fruit Pulp; Cupric Sulfate; Gelsemium Sempervirens Root; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Recutita; Passiflora Incarnata Flowering Top; Veratrum Album Root
Usage Information:
Adults and children 12 years and older: Chew 2 tablets every 4 hours, or use as directed by you health professional. Children 4 to 11 years: Chew 1-2 tablets every 4 hours,or as directed by your health professional . For children under 4 years, use as directed by your health professional.
11-Digit NDC Billing Format:
62795104002
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
90 EA
Product Type:
Human Otc Drug
Labeler Name:
Medinatura Inc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACONITUM NAPELLUS 6 [hp_X]/1
  • AMANITA MUSCARIA FRUITING BODY 4 [hp_X]/1
  • AMMONIUM BROMIDE 4 [hp_X]/1
  • ATROPA BELLADONNA 6 [hp_X]/1
  • ATROPINE SULFATE 6 [hp_X]/1
  • CITRULLUS COLOCYNTHIS FRUIT PULP 3 [hp_X]/1
  • CUPRIC SULFATE 6 [hp_X]/1
  • GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/1
  • MATRICARIA RECUTITA 2 [hp_X]/1
  • PASSIFLORA INCARNATA FLOWERING TOP 2 [hp_X]/1
  • VERATRUM ALBUM ROOT 5 [hp_X]/1
    • Pharmacologic Class(es):
  • Anticholinergic - [EPC] (Established Pharmacologic Class)
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cholinergic Antagonists - [MoA] (Mechanism of Action)
  • Cholinergic Muscarinic Antagonist - [EPC] (Established Pharmacologic Class)
  • Cholinergic Muscarinic Antagonists - [MoA] (Mechanism of Action)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-16-2017
    End Marketing Date:
    04-30-2025
    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 62795-1040-2?

    The NDC Packaged Code 62795-1040-2 is assigned to a package of 90 tablet in 1 bottle of T-relief Pro Spasm, a human over the counter drug labeled by Medinatura Inc. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 90 billable units per package.

    Is NDC 62795-1040 included in the NDC Directory?

    Yes, T-relief Pro Spasm with product code 62795-1040 is active and included in the NDC Directory. The product was first marketed by Medinatura Inc on November 16, 2017.

    What is the NDC billing unit for package 62795-1040-2?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 90.

    What is the 11-digit format for NDC 62795-1040-2?

    The 11-digit format is 62795104002. 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
    5-4-162795-1040-25-4-262795-1040-02