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Jet Lag Anacardium orientale, Apis mellifica, Carbo vegetabilis, Carduus marianus, Cocculus indicus, Kali phosphoricum, Nux vomica, Passiflora incarnata, Phosphoricum acidum, Tabacum, 12 [hp_X]/mL; 200 [hp_C]/mL; 200 [hp_C]/mL; 3 [hp_X]/mL; 30 [hp_C]/mL; 12 [hp_X]/mL; 30 [hp_C Spray — NDC 50845-0032-2 (Billing 50845-0032-02)

by Liddell Laboratories, Inc. · 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY

This is a package of Jet Lag Anacardium orientale, Apis mellifica, Carbo vegetabilis, Carduus marianus, Cocculus indicus, Kali phosphoricum, Nux vomica, Passiflora incarnata, Phosphoricum acidum, Tabacum, 12 [hp_X]/mL; 200 [hp_C]/mL; 200 [hp_C]/mL; 3 [hp_X]/mL; 30 [hp_C]/mL; 12 [hp_X]/mL; 30 [hp_C Spray from Liddell Laboratories, Inc., marketed since Jun 2011 and currently FDA-listed. It is this product's only package size.

NDC 50845-0032-02
🏷️ FDA NDC (as labeled) 50845-0032-2 billing pads the package segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 50845-0032-2
Product NDC 50845-0032
11-digit billing NDC 50845003202
UNII Y0F0BU8RDU, 7S82P3R43Z, 2P3VWU3H10, U946SH95EE, 810258W28U, CI71S98N1Z +4 more
UPC 0363113275964
SPL Set ID 2bb38633-95a8-4db2-b4e8-8fc2fdbb5221
Established class (EPC) Standardized Insect Venom Allergenic Extract; Non-Standardized Plant Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Bee Venoms; Plant Proteins; Seed Storage Proteins
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-06-02
Route ORAL
Dosage form SPRAY
Substance SEMECARPUS ANACARDIUM JUICE; APIS MELLIFERA; ACTIVATED CHARCOAL; SILYBUM MARIANUM SEED; ANAMIRTA COCCULUS SEED; POTASSIUM PHOSPHATE, DIBASIC; STRYCHNOS NUX-VOMICA SEED; PASSIFLORA INCARNATA TOP; PHOSPHORIC ACID; TOBACCO LEAF
Why two NDCs? The FDA registers this code as 50845-0032-2 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 50845-0032-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

This is an unapproved homeopathic spray product taken by mouth, containing multiple plant and mineral extracts combined according to homeopathic tradition. The formula includes activated charcoal (typically used in homeopathy for digestive symptoms), Passiflora and Nux vomica (commonly included in homeopathic preparations for sleep and nervousness), Phosphoric acid and Potassium phosphate (used in homeopathic practice for fatigue), and other plant extracts. Homeopathic products are marketed based on traditional use rather than clinical evidence, and the FDA does not evaluate them for effectiveness.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
50845-0032-02 You're viewing this Main listing 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY 2016-11-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Jet Lag 12 [hp_X]/mL; 200 [hp_C]/mL; 200 [hp_C]/mL; 3 [hp_X]/mL; 30 [hp_C]/mL; 12 [hp_X]/mL; 30 [hp_Cthis 50845-0032-02 Liddell 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2011
On the market since
Jun 2011
📍
2026
Currently FDA-listed
15 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerLiddell Laboratories, Inc.
Labeler code50845
First marketedJun 2011
Product typeHuman Otc Drug
Portfolio52 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 43 words ▾

USES: For use during and after jet travel as it may help temporarily relieve the symptoms commonly known as "jet lag", such as tiredness, feelings of disorientation, dehydration, and sleeplessness.** **Claims based upon traditional homeopathic practice, not accepted medical evidence. Not FDA Evaluated.

⏱️ Dosage and Administration 42 words ▾

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.

⚠️ Warnings 90 words ▾

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 for more than 7 days, 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.

Store at room temperature.

🧪 Active Ingredient 36 words ▾

ACTIVE INGREDIENTS: (in each spray): 10% of Anacardium orientale 12X, Apis mellifica 200C, Carbo vegetabilis 200C, Carduus marianus 3X, Cocculus indicus 30C, Kali phosphoricum 12X, Nux vomica 30C, Passiflora incarnata 1X, Phosphoricum acidum 200C, Tabacum 6X.

🧪 Inactive Ingredients 8 words ▾

INACTIVE INGREDIENTS: Organic alcohol 20% v/v, Purified water.

🎯 Purpose 28 words ▾

USES: May temporarily relieve symptoms of jet lag, including: tiredness feelings of disorientation dehydration sleeplessness** **Claims based upon traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

📄 Keep Out of Reach of Children 21 words ▾

KEEP OUT OF REACH OF CHILDREN: In case of overdose, get medical help or call a Poison Control Center right away.

📄 Questions or Comments 14 words ▾

QUESTIONS: DIST. BY LIDDELL LABORATORIES, INC. 201 APPLE BLVD. WOODBINE, IA 51579 WWW.LIDDELL.NET 1-800-460-7733

📄 Package Label / Principal Display Panel 51 words ▾

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Jet Lag Anacardium orientale, Apis mellifica, Carbo vegetabilis, Carduus marianus, Cocculus indicus, Kali phosphoricum, Nux vomica, Passiflora incarnata, Phosphoricum acidum, Tabacum, 12 [hp_X]/mL; 200 [hp_C]/mL; 200 [hp_C]/mL; 3 [hp_X]/mL; 30 [hp_C]/mL; 12 [hp_X]/mL; 30 [hp_C SPRAY is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Liddell Laboratories, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Liddell Laboratories, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 50844-0991-26 · L.N.K. 50845-0047-02 · Liddell →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.