70163-0005 NDC - LEG CRAMPS (CHININUM SULPHURICUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, CALCAREA CARBONICA, RHUS TOX, CUPRUM METALLICUM)

Drug Information

  • Product NDC: 70163-0005
  • Proprietary Name: Leg Cramps
  • Non Proprietary Name: Chininum Sulphuricum, Colocynthis, Gnaphalium Polycephalum, Lycopodium Clavatum, Magnesia Phosphorica, Calcarea Carbonica, Rhus Tox, Cuprum Metallicum
  • Active Ingredient(s): 4 [hp_X]/1 CITRULLUS COLOCYNTHIS FRUIT PULP; 12 [hp_X]/1 COPPER; 6 [hp_X]/1 LYCOPODIUM CLAVATUM SPORE; 6 [hp_X]/1 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; 6 [hp_X]/1 OYSTER SHELL CALCIUM CARBONATE, CRUDE; 4 [hp_X]/1 PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; 4 [hp_X]/1 QUININE SULFATE; 6 [hp_X]/1 TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET
  • Pharmacy Class(es): Antimalarial [EPC]; Calculi Dissolution Agent [EPC]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibit Ovum Fertilization [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Field Name Field Value
Labeler Name: NaturalCare
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/3/2026

Package Information

No. Package Code Package Description Billing Unit
170163-0005-11 BLISTER PACK in 1 CONTAINER (70163-0005-1) / 60 TABLET in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC70163-0005The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELeg CrampsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEChininum Sulphuricum, Colocynthis, Gnaphalium Polycephalum, Lycopodium Clavatum, Magnesia Phosphorica, Calcarea Carbonica, Rhus Tox, Cuprum MetallicumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/3/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMENaturalCareName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECITRULLUS COLOCYNTHIS FRUIT PULP; COPPER; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; QUININE SULFATE; TOXICODENDRON PUBESCENS LEAFAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH4; 12; 6; 6; 6; 4; 4; 6 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 
PHARM CLASSESAntimalarial [EPC], Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 3/6/2026

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