NDC 60986-1014 Contessa
Alchemilla Vulgaris, Asperula Odorata, Chamomilla, Viola Odorata, Cinchona Officinalis...

Product Information

What is NDC 60986-1014?

The NDC code 60986-1014 is assigned by the FDA to the product Contessa which is a human over the counter drug product labeled by Marco Pharma International Llc.. The generic name of Contessa is alchemilla vulgaris, asperula odorata, chamomilla, viola odorata, cinchona officinalis, mentha piperita, rosmarinus officinalis, valeriana officinalis, helonia dioica, agnus castus, ambra grisea, cimicifuga racemosa, convallaria majalis, crocus sativus, cyclamen europaeum, damiana, hydrastis canadensis, caulophyllum thalictroides, lilium tigrinum, senecio aureus, staphysagria, naja tripudians. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 60986-1014-7 236 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code60986-1014
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name 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.
Alchemilla Vulgaris, Asperula Odorata, Chamomilla, Viola Odorata, Cinchona Officinalis, Mentha Piperita, Rosmarinus Officinalis, Valeriana Officinalis, Helonia Dioica, Agnus Castus, Ambra Grisea, Cimicifuga Racemosa, Convallaria Majalis, Crocus Sativus, Cyclamen Europaeum, Damiana, Hydrastis Canadensis, Caulophyllum Thalictroides, Lilium Tigrinum, Senecio Aureus, Staphysagria, Naja Tripudians
Product Type 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.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Oral - Administration to or by way of the mouth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Marco Pharma International Llc.
Labeler Code60986
Marketing Category 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.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 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.
Exclude Flag 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".
NDC Code Structure

What are the uses for Contessa?

Product Packages

NDC Code 60986-1014-7

Package Description: 236 mL in 1 BOTTLE, GLASS

Product Details

What are Contessa 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.

Contessa Active Ingredients UNII Codes

Contessa 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.

* Please review the disclaimer below.

Contessa Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Active Ingredients

Alchemilla Vulgaris 1x

Asperula Odorata 1xHPUS

Chamomilla 1xHPUS

Viola Odorata 1xHPUS

Cinchona Officinalis 2x

Mentha Piperita 1xHPUS

Rosmarinus Officinalis 1xHPUS

Valeriana Officinalis 1xHPUS

Helonias Dioica 2xHPUS

Agnus Castus 3XHPUS

Ambra Grisea 3xHPUS

Cimicifuga Racemosa 3xHPUS

Convalleria Majalis 3xHPUS

Crocus Sativus 3xHPUS

Cyclamen Europaeum 3xHPUS

Damiana 3xHPUS

Hydrastis Canadensis 3xHPUS

Caulophyllum Thalictroides 4xHPUS

Lilium Tigrinum 4xHPUS

Senecio Aureus 4xHPUS

Staphysagria 4xHPUS

Naja Tripudians 8xHPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.


For fatigue, mental and physical exhaustion, PMS, depression and irritability.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Suggested Use

Adults take 1 tablespoon two to three times daily. Children 12 to 18 years of age take 1 teaspoon two to three times daily. Not intended for children under 12 years of age.


If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

Dosage & Administration

(Read Suggested Use Section)

Inactive Ingredients

Ethyl Alcohol (20.9% by vol.) and Water

Package Label.Principal Display Panel

female tonic

* Please review the disclaimer below.