FDA.reportPublic FDA data

Jet Lag

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2024-05-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:27:00

Label at a glance#

ProductJet Lag
Active ingredientSEMECARPUS 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
Label structure9 sections

Indications and 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.

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(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.

USES:

OTC - PURPOSE SECTION

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.

WARNINGS:

WARNINGS SECTION

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.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or call a Poison Control Center right away.

USES:

INDICATIONS & USAGE SECTION

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.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY

LIDDELL LABORATORIES, INC.

201 APPLE BLVD.

WOODBINE, IA 51579

www.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 lblJet Lag lbl

Jet Lag ctnJet Lag ctn

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
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810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
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ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0032-22024-05-21C16284748780-1ba0f9c33-3990-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0032-22024-01-30C16284748780-1ba0f9c33-3990-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0032-22022-05-13C16284748780-1ba0f9c33-3990-a910-e053-dadaa90a0b85DRUG FACTS:
50845-0032-22021-01-29C16284748780-1ba0f9c33-3990-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50845-0032-1Jet Lag30 mL in 1 BOTTLE, SPRAYSPRAY306
50845-0032-2Jet Lag1 in 1 CARTONSPRAY16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50845-0032JET LAG (ANACARDIUM ORIENTALE, APIS MELLIFICA, CARBO VEGETABILIS, CARDUUS MARIANUS, COCCULUS INDICUS, KALI PHOSPHORICUM, NUX VOMICA, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, TABACUM,) SPRAY [LIDDELL LABORATORIES, INC.]6Current NDC, Legacy NDC, 2 package rows20240522_2bb38633-95a8-4db2-b4e8-8fc2fdbb5221.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H102
ANAMIRTA COCCULUS SEEDACTIVE INGREDIENT810258W28U2
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z2
PASSIFLORA INCARNATA TOPACTIVE INGREDIENTCLF5YFS11O2
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN2
POTASSIUM PHOSPHATE, DIBASICACTIVE INGREDIENTCI71S98N1Z2
SEMECARPUS ANACARDIUM JUICEACTIVE INGREDIENTY0F0BU8RDU2
SILYBUM MARIANUM SEEDACTIVE INGREDIENTU946SH95EE2
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139192
TOBACCO LEAFACTIVE INGREDIENT6YR2608RSU2
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H102
ANAMIRTA COCCULUS SEEDACTIVE MOIETY810258W28U2
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z2
PASSIFLORA INCARNATA TOPACTIVE MOIETYCLF5YFS11O2
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN2
POTASSIUM CATIONACTIVE MOIETY295O53K1522
SEMECARPUS ANACARDIUM JUICEACTIVE MOIETYY0F0BU8RDU2
SILYBUM MARIANUM SEEDACTIVE MOIETYU946SH95EE2
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139192
TOBACCO LEAFACTIVE MOIETY6YR2608RSU2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-003250845-0032-1, 50845-0032-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
SEMECARPUS ANACARDIUM JUICEY0F0BU8RDUACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
SILYBUM MARIANUM SEEDU946SH95EEACTIB
ANAMIRTA COCCULUS SEED810258W28UACTIB
POTASSIUM PHOSPHATE, DIBASICCI71S98N1ZACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PASSIFLORA INCARNATA TOPCLF5YFS11OACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
TOBACCO LEAF6YR2608RSUACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 45 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii+dosage form
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
45 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
45 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Jet LagANACARDIUM ORIENTALE, APIS MELLIFICA, CARBO VEGETABILIS, CARDUUS MARIANUS, COCCULUS INDICUS, KALI PHOSPHORICUM, NUX VOMICA, PASSIFLORA INCARNATA, PHOSPHORICUM ACIDUM, TABACUM,Liddell Laboratories, Inc.2bb38633-95a8-4db2-b4e8-8fc2fdbb52212024-05-20WarningsExact identifier
ndc (package): 50845-0032-1
ndc (package): 50845-0032-2
ndc (product): 50845-0032
ndc11 (package): 50845003201
ndc11 (package): 50845003202
spl id: f967d18c-e2ff-471e-9769-9f00242f9b0e
spl set id: 2bb38633-95a8-4db2-b4e8-8fc2fdbb5221

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.