Ohm Drainage Lymphatic

Aesculus Hipp, Apis Mel, Aranea, Baryta Carb, Equisetum Hyem, Fucus, Fumaria, Juglans Cin, Kali Iod, Kali Mur, Myosotis, Nasturtium, Nat Sulphuricum, Phytolacca, Sarsaparilla, Scrophulara, Secale, Teucrium Scor, Thyroidinum, Vipera.

Ohm Pharma Inc.
Human Otc Drug
NDC 66096-695

Ohm Drainage Lymphatic also known as Aesculus Hipp, Apis Mel, Aranea, Baryta Carb, Equisetum Hyem, Fucus, Fumaria, Juglans Cin, Kali Iod, Kali Mur, Myosotis, Nasturtium, Nat Sulphuricum, Phytolacca, Sarsaparilla, Scrophulara, Secale, Teucrium Scor, Thyroidinum, Vipera. is a human otc drug labeled by 'Ohm Pharma Inc.'. National Drug Code (NDC) number for Ohm Drainage Lymphatic is 66096-695. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Ohm Drainage Lymphatic drug includes Apis Mellifera - 4 [hp_X]/100g Araneus Diadematus - 14 [hp_X]/100g Barium Carbonate - 14 [hp_X]/100g Claviceps Purpurea Sclerotium - 6 [hp_X]/100g Equisetum Hyemale - 3 [hp_X]/100g Fucus Vesiculosus - 3 [hp_X]/100g Fumaria Officinalis Flowering Top - 2 [hp_X]/100g Horse Chestnut - 4 [hp_X]/100g Juglans Cinerea Branch Bark/root Bark - 2 [hp_X]/100g Myosotis Arvensis - 2 [hp_X]/100g and more. The currest status of Ohm Drainage Lymphatic drug is Active.

Drug Information:

Drug NDC:	66096-695
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:	Ohm Drainage Lymphatic
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:	Aesculus Hipp, Apis Mel, Aranea, Baryta Carb, Equisetum Hyem, Fucus, Fumaria, Juglans Cin, Kali Iod, Kali Mur, Myosotis, Nasturtium, Nat Sulphuricum, Phytolacca, Sarsaparilla, Scrophulara, Secale, Teucrium Scor, Thyroidinum, Vipera.
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Ohm Pharma Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Gel
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:	APIS MELLIFERA - 4 [hp_X]/100g ARANEUS DIADEMATUS - 14 [hp_X]/100g BARIUM CARBONATE - 14 [hp_X]/100g CLAVICEPS PURPUREA SCLEROTIUM - 6 [hp_X]/100g EQUISETUM HYEMALE - 3 [hp_X]/100g FUCUS VESICULOSUS - 3 [hp_X]/100g FUMARIA OFFICINALIS FLOWERING TOP - 2 [hp_X]/100g HORSE CHESTNUT - 4 [hp_X]/100g JUGLANS CINEREA BRANCH BARK/ROOT BARK - 2 [hp_X]/100g MYOSOTIS ARVENSIS - 2 [hp_X]/100g Load more... NASTURTIUM OFFICINALE - 2 [hp_X]/100g PHYTOLACCA AMERICANA ROOT - 2 [hp_X]/100g POTASSIUM CHLORIDE - 2 [hp_X]/100g POTASSIUM IODIDE - 2 [hp_X]/100g SCROPHULARIA NODOSA - 3 [hp_X]/100g SMILAX ORNATA ROOT - 2 [hp_X]/100g SODIUM SULFATE - 2 [hp_X]/100g TEUCRIUM SCORODONIA FLOWERING TOP - 2 [hp_X]/100g THYROID, UNSPECIFIED - 10 [hp_X]/100g VIPERA BERUS VENOM - 6 [hp_X]/100g
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
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:	16 Dec, 2014
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	18 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:	OHM PHARMA INC.
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.
UPC:	0366096695101
UPC stands for Universal Product Code.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	7S82P3R43Z 6T6CO7R3Z5 6P669D8HQ8 01G9XEA93N 59677RXH25 535G2ABX9M VH659J61ZL 3C18L6RJAZ 48FZ1BHO18 C73BK97H5J Load more... YH89GMV676 11E6VI8VEG 660YQ98I10 1C4QK22F9J 7H443NUB2T 2H1576D5WG 0YPR65R21J LOK3I16O7G 0B4FDL9I6P 0ORO6NCA4M
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.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Bee Venoms [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Osmotic Activity [MoA] Osmotic Laxative [EPC] Potassium Compounds [CS] Potassium Salt [EPC] Standardized Insect Venom Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
66096-695-10	100 g in 1 TUBE (66096-695-10)	16 Dec, 2014	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.

Other medicines with the same generic name

Ohm Drainage Lymphatic

Aesculus Hipp & more..

Gel
OHM PHARMA INC.
NDC: 66096-695

Purpose:

Relieves slow lymphatic drainage, assists in removing toxins and improves metabolism.

Product Elements:

Ohm drainage lymphatic aesculus hipp, apis mel, aranea, baryta carb, equisetum hyem, fucus, fumaria, juglans cin, kali iod, kali mur, myosotis, nasturtium, nat sulphuricum, phytolacca, sarsaparilla, scrophulara, secale, teucrium scor, thyroidinum, vipera. carbomer 940 alcohol glycerin water sodium hydroxymethylglycinate horse chestnut horse chestnut apis mellifera apis mellifera araneus diadematus araneus diadematus barium carbonate barium cation equisetum hyemale equisetum hyemale fucus vesiculosus fucus vesiculosus fumaria officinalis flowering top fumaria officinalis flowering top juglans cinerea branch bark/root bark juglans cinerea branch bark/root bark potassium iodide iodide ion potassium chloride potassium cation myosotis arvensis myosotis arvensis nasturtium officinale nasturtium officinale sodium sulfate sodium sulfate anhydrous phytolacca americana root phytolacca americana root smilax ornata root sarsaparilla scrophularia nodosa scrophularia nodosa claviceps purpurea sclerotium claviceps purpurea sclerotium teucrium scorodonia flowering top teucrium scorodonia flowering top thyroid, unspecified thyroid, unspecified vipera berus venom vipera berus venom

Indications and Usage:

Uses: temporarily relieves slow lymphatic drainage. assists in removing toxins and improves metabolism.** â**claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: for topical use only. do not apply to broken skin. if pregnant or breast-feeding, ask a health professional before use. if symptoms worsen or persist for more than 5 days, discontinue use and contact a health care professional. in case of overdose (or accidental ingestion) get medical help or contact a poison control center right away. âkeep out of reach of children.

Dosage and Administration:

Directions: apply a small amount to affected area 3 times a day or as directed by a health care professional.

Package Label Principal Display Panel:

Ndc: 66096-695-10 ohm drainage lymphatic gel natural - safe - effective no side effects topical homeopathic net wt: 3.5 oz (100 g) made in usa 3.5oz tube label relieves slow lymphatic drainage, assists in removing toxins and improves metabolism.

Further Questions:

Mfg. by: ohm pharma, inc. mineral wells, tx 76067 www.ohmpharma.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.