NDC 43857-0206 Rhustoxoforce

NDC Product Code 43857-0206

NDC 43857-0206-1

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

Rhustoxoforce with NDC 43857-0206 is a product labeled by Bioactive Nutritional, Inc.. The generic name of Rhustoxoforce is . The product's dosage form is and is administered via form.

Labeler Name: Bioactive Nutritional, 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: Bioactive Nutritional, Inc.
Labeler Code: 43857
Start Marketing Date: 08-21-2013 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’.

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Rhustoxoforce Product Label Images

Rhustoxoforce 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 12X, Cantharis 12X, Graphites 12X, Natrum Muriaticum 12X, Rhus Glabra 12X, Rhus Toxidodendron 12X, Rhus Venenata 12X, Urtica Dioica 12X

Indications:

For temporary relief of allergies caused by poison ivy, oak, and summac.

For temporary relief of allergies caused by poison ivy, oak, and summac.

Warnings:

​If pregnant or breast-feeding,​ ask a health care professional befure 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:

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

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.

Questions:

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

Package Label Display:

BioActie HomeopathicRHUSTOXOFORCE1 FL OZ (30 mL)

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