1. Home
  2. Labeler Index
  3. Centered Enterprises, Llc
  4. NDC Product Code: 70105-002 Natural Relief Patch For Menstrual Cramps

NDC 70105-002 Natural Relief Patch For Menstrual Cramps

Belladonna,Calendula Officinalis,Chamomilla,Colocynthis,Magnesia Phosphorica,Nux - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70105-002?
  4. Natural Relief Patch For Menstrual Cramps Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
70105-002
Proprietary Name:
Natural Relief Patch For Menstrual Cramps
Non-Proprietary Name: [1]
Belladonna, Calendula Officinalis, Chamomilla, Colocynthis, Magnesia Phosphorica, Nux Vomica, Pulsatilla.
Substance Name: [2]
Atropa Belladonna; Calendula Officinalis Flowering Top; Citrullus Colocynthis Fruit Pulp; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Recutita; Pulsatilla Vulgaris; Strychnos Nux-vomica Seed
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Centered Enterprises, Llc
    Labeler Code:
    70105
    Product Label ID:
    82162b47-b614-459f-8129-3fdece8853f6
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-14-2015
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 70105-002?

    The NDC code 70105-002 is assigned by the FDA to the product Natural Relief Patch For Menstrual Cramps which is a human over the counter drug product labeled by Centered Enterprises, Llc. The generic name of Natural Relief Patch For Menstrual Cramps is belladonna, calendula officinalis, chamomilla, colocynthis, magnesia phosphorica, nux vomica, pulsatilla.. The product's dosage form is patch and is administered via topical form. The product is distributed in a single package with assigned NDC code 70105-002-05 5 patch in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Natural Relief Patch For Menstrual Cramps?

    Uses*Relieves symptoms of menstrual cramping and discomfort associated with the menstrual period.

    What are Natural Relief Patch For Menstrual Cramps Active Ingredients?

    An 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.

    Which are Natural Relief Patch For Menstrual Cramps UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
    • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
    • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
    • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
    • PULSATILLA VULGARIS (UNII: I76KB35JEV)
    • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)

    Which are Natural Relief Patch For Menstrual Cramps Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Natural Relief Patch For Menstrual Cramps?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An 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.

    [3] What kind of product is this? - Indicates 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".