NDC 60986-1004 Lymphonest

Echinacea Augustifolia, Scrophularia Nodosa, Abrotanum, Petroleum, Aloe Socotrina, Mercurius Solubilis, Crotalus Horiidus, Thuja Occidentalis, Lachesis Mutus, Aristolochia Clematitis

NDC Product Code 60986-1004

NDC CODE: 60986-1004

Proprietary Name: Lymphonest 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: Echinacea Augustifolia, Scrophularia Nodosa, Abrotanum, Petroleum, Aloe Socotrina, Mercurius Solubilis, Crotalus Horiidus, Thuja Occidentalis, Lachesis Mutus, Aristolochia Clematitis 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.

NDC Code Structure

NDC 60986-1004-3

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC 60986-1004-4

Package Description: 100 mL in 1 PACKAGE

NDC Product Information

Lymphonest with NDC 60986-1004 is a a human over the counter drug product labeled by Marco Pharma International Llc.. The generic name of Lymphonest is echinacea augustifolia, scrophularia nodosa, abrotanum, petroleum, aloe socotrina, mercurius solubilis, crotalus horiidus, thuja occidentalis, lachesis mutus, aristolochia clematitis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Marco Pharma International Llc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Lymphonest Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • KEROSENE 3 [hp_X]/100mL
  • ALOE 1 [hp_X]/100mL
  • LACHESIS MUTA VENOM 8 [hp_X]/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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.

Labeler Name: Marco Pharma International Llc.
Labeler Code: 60986
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 03-01-1992 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: 12-31-2021 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: N - NO 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".

* Please review the disclaimer below.

Lymphonest Product Label Images

Lymphonest Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Coneflower 1x HPUSFigwort 1x HPUSSouthernwood 3x HPUSKerosine 3x HPUSCape Aloe 1x HPUSHahnemann's soluble mercury 12x HPUSTimber rattlesnake 10x HPUSWhite cedar 10x HPUSBushmaster Viper 8x HPUSBirthwort 6x HPUSThe letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.


For relief of swollen lymph glands; suppressed immune functions.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Suggested Use

30 drops in water 3 times daily. In acute stages, take 50 drops at once followed by 30 drops 4 times daily. Children receive one half or less of the adult amount.


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 (63% by vol.) and Water

* Please review the disclaimer below.