Hevert Detox Lymph
Arsenic Trioxide, Clematis Recta Flowering Top, Conium Maculatum Flowering Top, Lachesis Muta Venom, Mercuric Iodide, Phytolacca Americana Root, Toxicodendron Pubescens Shoot, Scrophularia Nodosa Leaf With Stem, And Sulfur
Hevert Arzneimittel Gmbh & Co Kg
Human Otc Drug
NDC 54532-0034Hevert Detox Lymph also known as Arsenic Trioxide, Clematis Recta Flowering Top, Conium Maculatum Flowering Top, Lachesis Muta Venom, Mercuric Iodide, Phytolacca Americana Root, Toxicodendron Pubescens Shoot, Scrophularia Nodosa Leaf With Stem, And Sulfur is a human otc drug labeled by 'Hevert Arzneimittel Gmbh & Co Kg'. National Drug Code (NDC) number for Hevert Detox Lymph is 54532-0034. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Hevert Detox Lymph drug includes Arsenic Trioxide - 6 [hp_X]/50mL Clematis Recta Flowering Top - 4 [hp_X]/50mL Conium Maculatum Flowering Top - 6 [hp_X]/50mL Lachesis Muta Venom - 8 [hp_X]/50mL Mercuric Iodide - 8 [hp_X]/50mL Phytolacca Americana Root - 4 [hp_X]/50mL Scrophularia Nodosa Leaf With Stem - 3 [hp_X]/50mL Sulfur - 4 [hp_X]/50mL Toxicodendron Pubescens Shoot - 6 [hp_X]/50mL . The currest status of Hevert Detox Lymph drug is Active.
Drug Information:
| Drug NDC: | 54532-0034 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Hevert Detox Lymph |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Arsenic Trioxide, Clematis Recta Flowering Top, Conium Maculatum Flowering Top, Lachesis Muta Venom, Mercuric Iodide, Phytolacca Americana Root, Toxicodendron Pubescens Shoot, Scrophularia Nodosa Leaf With Stem, And Sulfur |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Hevert Arzneimittel Gmbh & Co Kg |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | ARSENIC TRIOXIDE - 6 [hp_X]/50mL
CLEMATIS RECTA FLOWERING TOP - 4 [hp_X]/50mL
CONIUM MACULATUM FLOWERING TOP - 6 [hp_X]/50mL
LACHESIS MUTA VENOM - 8 [hp_X]/50mL
MERCURIC IODIDE - 8 [hp_X]/50mL
PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/50mL
SCROPHULARIA NODOSA LEAF WITH STEM - 3 [hp_X]/50mL
SULFUR - 4 [hp_X]/50mL
TOXICODENDRON PUBESCENS SHOOT - 6 [hp_X]/50mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | ORAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 15 Jun, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 13 Jun, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Hevert Arzneimittel GmbH & Co KG
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | S7V92P67HO
396421SP9F
Q28R5GF371
VSW71SS07I
R03O05RB0P
11E6VI8VEG
K93UPA2CNQ
70FD1KFU70
46PYZ1F82M
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 54532-0034-5 | 1 BOTTLE in 1 CARTON (54532-0034-5) / 50 mL in 1 BOTTLE | 15 Jun, 2016 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Active ingredients purpose "x" indicates a homeopathic dilution. for more information visit: www.hevertusa.com arsenicum album 6x relief of discomfort associated with lymphatic swelling and edema clematis 4x conium 6x lachesis 8x mercurius bijodatus 8x phytolacca 4x rhus toxicodendron 6x scrophularia nodosa, herba 3x sulfur 4x
Product Elements:
Hevert detox lymph arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens shoot, scrophularia nodosa leaf with stem, and sulfur arsenic trioxide arsenic cation (3+) clematis recta flowering top clematis recta flowering top conium maculatum flowering top conium maculatum flowering top lachesis muta venom lachesis muta venom mercuric iodide mercuric iodide phytolacca americana root phytolacca americana root toxicodendron pubescens shoot toxicodendron pubescens shoot scrophularia nodosa leaf with stem scrophularia nodosa leaf with stem sulfur sulfur alcohol water
Indications and Usage:
Uses for temporary relief of discomfort associated with lymphatic swelling and edema. claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.
Warnings:
Warnings for oral use only. chronically enlarged lymph nodes can be the sign of different diseases. therefore, consult a doctor in order to clarify the underlying disease before using this medicine. also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment. do not use if you are allergic to rhus toxicodendron or other plants from the cashew family stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur. 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:
Warnings for oral use only. chronically enlarged lymph nodes can be the sign of different diseases. therefore, consult a doctor in order to clarify the underlying disease before using this medicine. also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment. do not use if you are allergic to rhus toxicodendron or other plants from the cashew family stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur. 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.
Dosage and Administration:
Directions adults and children over 12 years of age: take 20 drops in water 3 times daily. consult a physician for use in children under 12 years of age. do not use for children under 1 year of age.
Stop Use:
Stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.
Package Label Principal Display Panel:
Principal display panel - 50 ml bottle carton ndc 54532-0034-5 hevert ® detox lymph homeopathic medicine for the lymphatic system 1.7 fl oz (50 ml) 46 % alcohol v/v oral drops made in germany hevert principal display panel - 50 ml bottle carton
Further Questions:
Questions? 1-855-387-6466