Jet Lag

Anacardium Orientale, Apis Mellifica, Carbo Vegetabilis, Carduus Marianus, Cocculus Indicus, Kali Phosphoricum, Nux Vomica, Passiflora Incarnata, Phosphoricum Acidum, Tabacum,

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0032

Jet Lag also known as Anacardium Orientale, Apis Mellifica, Carbo Vegetabilis, Carduus Marianus, Cocculus Indicus, Kali Phosphoricum, Nux Vomica, Passiflora Incarnata, Phosphoricum Acidum, Tabacum, is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Jet Lag is 50845-0032. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Jet Lag drug includes Activated Charcoal - 200 [hp_C]/mL Anamirta Cocculus Seed - 30 [hp_C]/mL Apis Mellifera - 200 [hp_C]/mL Passiflora Incarnata Top - 1 [hp_X]/mL Phosphoric Acid - 200 [hp_C]/mL Potassium Phosphate, Dibasic - 12 [hp_X]/mL Semecarpus Anacardium Juice - 12 [hp_X]/mL Silybum Marianum Seed - 3 [hp_X]/mL Strychnos Nux-vomica Seed - 30 [hp_C]/mL Tobacco Leaf - 6 [hp_X]/mL . The currest status of Jet Lag drug is Active.

Drug Information:

Drug NDC:	50845-0032
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:	Jet Lag
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:	Anacardium Orientale, Apis Mellifica, Carbo Vegetabilis, Carduus Marianus, Cocculus Indicus, Kali Phosphoricum, Nux Vomica, Passiflora Incarnata, Phosphoricum Acidum, Tabacum,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Spray
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:	ACTIVATED CHARCOAL - 200 [hp_C]/mL ANAMIRTA COCCULUS SEED - 30 [hp_C]/mL APIS MELLIFERA - 200 [hp_C]/mL PASSIFLORA INCARNATA TOP - 1 [hp_X]/mL PHOSPHORIC ACID - 200 [hp_C]/mL POTASSIUM PHOSPHATE, DIBASIC - 12 [hp_X]/mL SEMECARPUS ANACARDIUM JUICE - 12 [hp_X]/mL SILYBUM MARIANUM SEED - 3 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 30 [hp_C]/mL TOBACCO LEAF - 6 [hp_X]/mL
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:	02 Jun, 2011
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:	Liddell Laboratories, 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:	0363113275964
UPC stands for Universal Product Code.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 N0000185375 M0016962 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	2P3VWU3H10 810258W28U 7S82P3R43Z CLF5YFS11O E4GA8884NN CI71S98N1Z Y0F0BU8RDU U946SH95EE 269XH13919 6YR2608RSU
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] Non-Standardized Plant 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] Plant Proteins [CS] Seed Storage Proteins [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] Non-Standardized Plant Allergenic Extract [EPC] Osmotic Activity [MoA] Osmotic Laxative [EPC] Plant Proteins [CS] Potassium Compounds [CS] Potassium Salt [EPC] Seed Storage Proteins [CS] 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
50845-0032-2	1 BOTTLE, SPRAY in 1 CARTON (50845-0032-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0032-1)	01 Nov, 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.

Other medicines with the same generic name

Jet Lag

Anacardium Orientale & more..

Spray
Liddell Laboratories, Inc.
NDC: 50845-0032

Purpose:

Uses: may temporarily relieve symptoms of jet lag, including: tiredness feelings of disorientation dehydration sleeplessness** **these statements are based upon traditional homeopathic practice. they have not been reviewed by the food and drug administration.

Product Elements:

Jet lag anacardium orientale, apis mellifica, carbo vegetabilis, carduus marianus, cocculus indicus, kali phosphoricum, nux vomica, passiflora incarnata, phosphoricum acidum, tabacum, semecarpus anacardium juice semecarpus anacardium juice apis mellifera apis mellifera activated charcoal activated charcoal silybum marianum seed silybum marianum seed anamirta cocculus seed anamirta cocculus seed potassium phosphate, dibasic potassium cation strychnos nux-vomica seed strychnos nux-vomica seed passiflora incarnata top passiflora incarnata top phosphoric acid phosphoric acid tobacco leaf tobacco leaf water alcohol

Indications and Usage:

Warnings:

Warnings: do not use if you have ever had an allergic reaction to this product or any of its ingredients. stop use and ask a doctor if symptoms persist, worsen, or if new symptoms occur. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. if pregnant or breast-feeding, ask a doctor before using product. do not use if tamper evident seal around neck of bottle is missing or broken. other information : store at room temperature.

Dosage and Administration:

Directions: adults and children over 12: two sprays under the tongue at departure, after each two hours of flight and upon landing. then two sprays three times a day until fully acclimated. children 12 and under: consult a doctor prior to use.

Package Label Principal Display Panel:

Package label display: oral sprays liddell laboratories est 1994 33 jlg jet lag may relieve symptoms of jet lag and may ease tiredness, dehydration, disorientation & sleeplessness. homeopathic doctor formulated readily absorbed. safe. no known side effects. easy to use 1.0 fl oz (30 ml) jet lag lbl jet lag ctn

Further Questions:

Questions: dist. by liddell laboratories, inc. 201 apple blvd woodbine, ia 51579 www.liddell.net 1-800-460-7733

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.