70105-002 NDC - NATURAL RELIEF PATCH FOR MENSTRUAL CRAMPS (BELLADONNA, CALENDULA OFFICINALIS, CHAMOMILLA, COLOCYNTHIS, MAGNESIA PHOSPHORICA, NUX VOMICA, PULSATILLA.)

Drug Information

Product NDC: 70105-002

Proprietary Name: Natural Relief Patch for MENSTRUAL CRAMPS

Non Proprietary Name: Belladonna, Calendula Officinalis, Chamomilla, Colocynthis, Magnesia Phosphorica, Nux Vomica, Pulsatilla.

Active Ingredient(s):
  • 15 [hp_C]/1 ATROPA BELLADONNA;
  • 3 [hp_X]/1 CALENDULA OFFICINALIS FLOWERING TOP;
  • 15 [hp_C]/1 CITRULLUS COLOCYNTHIS FRUIT PULP;
  • 15 [hp_C]/1 MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 3 [hp_X]/1 MATRICARIA RECUTITA;
  • 6 [hp_C]/1 PULSATILLA VULGARIS;
  • 6 [hp_C]/1 STRYCHNOS NUX-VOMICA SEED


Administration Route(s): TOPICAL

Dosage Form(s): PATCH

Pharmacy Class(es):
  • Allergens [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Labeler Name: Centered Enterprises, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/14/2015

Package Information

No. Package Code Package Description Billing Unit
170105-002-055 PATCH in 1 BOX (70105-002-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70105-002The 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 NAMENatural Relief Patch for MENSTRUAL 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 NAMEBelladonna, Calendula Officinalis, Chamomilla, Colocynthis, Magnesia Phosphorica, Nux Vomica, Pulsatilla.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/14/2015This 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 NAMECentered Enterprises, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; CITRULLUS COLOCYNTHIS FRUIT PULP; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA RECUTITA; PULSATILLA VULGARIS; STRYCHNOS NUX-VOMICA SEEDAn 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 STRENGTH15; 3; 15; 15; 3; 6; 6 
ACTIVE INGRED UNIT[hp_C]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1 
PHARM CLASSESAllergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 2/1/2023