NDC 43857-0299 Edema HP

Apis Mellifica, Arsenicum Album, Digitalis Purpurea, Ferrum Metallicum, Lycopodium Clavatum, Rhus Tox, Sambucus Nigra, Strophanthus Hispidus

NDC Product Code 43857-0299

NDC CODE: 43857-0299

Proprietary Name: Edema HP 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: Apis Mellifica, Arsenicum Album, Digitalis Purpurea, Ferrum Metallicum, Lycopodium Clavatum, Rhus Tox, Sambucus Nigra, Strophanthus Hispidus 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • This medication is an iron supplement used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.

NDC Code Structure

  • 43857 - Bioactive Nutritional, Inc.

NDC 43857-0299-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Edema HP with NDC 43857-0299 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Edema HP is apis mellifica, arsenicum album, digitalis purpurea, ferrum metallicum, lycopodium clavatum, rhus tox, sambucus nigra, strophanthus hispidus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, Inc.

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.

Edema HP 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.

  • APIS MELLIFERA 30 [hp_X]/mL
  • ARSENIC TRIOXIDE 30 [hp_X]/mL
  • DIGITALIS 30 [hp_X]/mL
  • IRON 30 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
  • SAMBUCUS NIGRA FLOWERING TOP 30 [hp_X]/mL
  • STROPHANTHUS HISPIDUS SEED 30 [hp_X]/mL

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)

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.
  • 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: Bioactive Nutritional, Inc.
Labeler Code: 43857
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: 06-03-2014 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 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.

Edema HP Product Label Images

Edema HP 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:

Apis Mellifica 3X, Arsenicum Album 30X, Digitalis Purpurea 30X, Ferrum Metallicum 30X, Lycopodium Clavatum 30X, Rhus Tox 30X, Sambucus Nigra 30X, Strophanthus Hispidus 30X.

Indications:

For temporary relief of symptoms of swelling of the extremities.

For temporary relief of symptoms of swelling of the extremities.

Warnings:

If pregnant or breast-feeding, ask a health care 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.

Keep Out Of Reach Of Children:

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

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Distributed by:BIOACTIVE NUTRITIONALMelbourne, FL 32935For Nutritional Information write:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935

Package Label Display:

BioActive HomeopathicEDEMA-HP1 FL OZ (30 ml)

* Please review the disclaimer below.