NDC 55146-006 6 Environmental Detox

6 Environmental Detox with NDC 55146-006 is a a human over the counter drug product labeled by Biotics Research Corporation. The generic name of 6 Environmental Detox is baptisia tinctoria, phytolacca decandra, spigelia anthelmia, adrenocorticotrophin, aluminum metallicum, apis mellifica, argentum nitricum, arsenicum album, benzoicum acidum, calcarea carbonica, carbo vegetabilis, kali phosphoricum, magnesia sulphurica, mercurius solubilis, nitricum acidum, nux vomica, phosphorus, silicea. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Biotics Research Corporation

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.

6 Environmental Detox 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.

• BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
• PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
• SPIGELIA ANTHELMIA 6 [hp_X]/mL
• CORTICOTROPIN 30 [hp_C]/mL
• ALUMINUM 30 [hp_C]/mL
• APIS MELLIFERA 30 [hp_C]/mL
• SILVER NITRATE 30 [hp_C]/mL
• ARSENIC TRIOXIDE 30 [hp_C]/mL
• BENZOIC ACID 30 [hp_C]/mL
• OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
• ACTIVATED CHARCOAL 30 [hp_C]/mL
• POTASSIUM PHOSPHATE, DIBASIC 30 [hp_C]/mL
• MAGNESIUM SULFATE HEPTAHYDRATE 30 [hp_C]/mL
• MERCURIUS SOLUBILIS 30 [hp_C]/mL
• NITRIC ACID 30 [hp_C]/mL
• STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL
• PHOSPHORUS 30 [hp_C]/mL
• SILICON DIOXIDE 30 [hp_C]/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)
• SODIUM BENZOATE (UNII: OJ245FE5EU)
• ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

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: Biotics Research Corporation
Labeler Code: 55146
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: 06-11-2019 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: 12-31-2020 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’.

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