1. Home
  2. Labeler Index
  3. Walgreen Company
  4. 0363-7174
  5. NDC Package Code: 0363-7174-14 Leg Cramps Pm

NDC Package 0363-7174-14 Leg Cramps Pm

Oyster Shell Calcium Carbonate,Crude,Causticum,Matricaria Recutita,Cinchona Officinalis - 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:
0363-7174-14
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 50 TABLET in 1 BOTTLE, PLASTIC
Product Code:
0363-7174
Proprietary Name:
Leg Cramps Pm
Non-Proprietary Name:
Oyster Shell Calcium Carbonate, Crude, Causticum, Matricaria Recutita, Cinchona Officinalis Bark, Copper, Lycopodium Clavatum Spore, Magnesium Phosphate, Dibasic Trihydrate, Toxicodendron Pubescens Leaf, Silicon Dioxide, And Sulfur
Substance Name:
Causticum; Cinchona Officinalis Bark; Copper; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Recutita; Oyster Shell Calcium Carbonate, Crude; Silicon Dioxide; Sulfur; Toxicodendron Pubescens Leaf
Usage Information:
• Suitable for adults and children ages 12 and over. Children under the age of 12: Consult a physician before use. Dissolve entire tablet under tongue OR chew tablet and swallow. • Do not swallow tablet whole. • Dissolve 1-2 tablets under tongue, every 4 hours or as needed. If the initial dosage is not providing relief, take 1-2 tablets every 15 minutes, for up to 6 doses. • Take at least 10 minutes before or at least 10 minutes after eating or drinking. • Homeopathic remedies may not be effective for everyone. Individual results may vary.
11-Digit NDC Billing Format:
00363717414
Product Type:
Human Otc Drug
Labeler Name:
Walgreen Company
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):
  • CAUSTICUM 12 [hp_X]/1
  • CINCHONA OFFICINALIS BARK 3 [hp_X]/1
  • COPPER 12 [hp_X]/1
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/1
  • MATRICARIA RECUTITA 6 [hp_X]/1
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/1
  • SILICON DIOXIDE 12 [hp_X]/1
  • SULFUR 6 [hp_X]/1
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/1
    • Pharmacologic Class(es):
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [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:
    05-21-2023
    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 0363-7174-14?

    The NDC Packaged Code 0363-7174-14 is assigned to a package of 1 bottle, plastic in 1 carton / 50 tablet in 1 bottle, plastic of Leg Cramps Pm, a human over the counter drug labeled by Walgreen Company. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0363-7174 included in the NDC Directory?

    Yes, Leg Cramps Pm with product code 0363-7174 is active and included in the NDC Directory. The product was first marketed by Walgreen Company on May 21, 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 0363-7174-14?

    The 11-digit format is 00363717414. 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 4-4-2 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
    4-4-20363-7174-145-4-200363-7174-14