NDC 44911-0076 Lymphdrainex

NDC Product Code 44911-0076

NDC 44911-0076-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Lymphdrainex with NDC 44911-0076 is a product labeled by Energique, Inc.. The generic name of Lymphdrainex is . The product's dosage form is and is administered via form.

Labeler Name: Energique, Inc.

Dosage Form: -

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.

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.

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

Product Labeler Information

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

Labeler Name: Energique, Inc.
Labeler Code: 44911
Start Marketing Date: 04-11-2013 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: 12-31-2019 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: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Lymphdrainex Product Label Images

Lymphdrainex 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

Geranium Robertianum 3X, 4X, Nasturtium Aquaticum 3X, 4X, Aloe Socotrina 3X, 4X, 6X, 8X, 12X, Juglans Regia 3X, 6X, Myosotis Arvensis 3X, 6X, Scrophularia Nodosa 3X, 6X, Teucrium Scorodonia 3X, 6X, Apis Mellifica 4X, Equisteum Hyemale 4X, Fumaria Officinalis 4X, Natrum Sulphuricum 4X, Phytolacca Decandra 4X, Pinus Sylvestris 4X, Veronic Officinalis 4X, Gentiana Lutea 5X, Sarsaparilla 6X, Baryta Carbonica 8X, Hepar Sulphuris Calcareum 8X, Mercurius Cyanatus 8X, Ferrum Iodatum 8X, 12X, Aranea Diadema 12X, Calcarea Phosphorica 12X, Parathyroid (Bovine) 12X, Thymus Suis 12X, Thyroidinum (Suis) 12X

Indications

For temporary relief of symptoms of acute or chronic lymphatic congestion; general immune support and lymphatic drainage. **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings

If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Directions

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

Demineralized water, 20% Ethanol.

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away.

Indications And Usage

For temporary relief of symptoms of acute or chronic lymphatic congestion; general immune support and lymphatic drainage.**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Questions

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579800-869-8078

* Please review the disclaimer below.