L-Trans

Manufacturer
Vitality Works, Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:10

Label at a glance#

ProductL-Trans
Active ingredientEUPATORIUM PERFOLIATUM FLOWERING TOP, FRAXINUS AMERICANA BARK, HYOSCYAMUS NIGER, LEDUM PALUSTRE TWIG, VERONICASTRUM VIRGINICUM ROOT, NICOTINE, SARSAPARILLA, TURPENTINE OIL, TEUCRIUM MARUM, CAPSELLA BURSA-PASTORIS, VIBURNUM OPULUS BARK, SILVER, ARNICA MONTANA, ARSENIC TRIIODIDE, BAPTISIA TINCTORIA, BENZENE, COBALT, CRATAEGUS FRUIT, SYZYGIUM JAMBOS SEED
Label structure8 sections

Label contents#

Full prescribing information#

L-Trans

OTC - ACTIVE INGREDIENT SECTION

Argentum Metallicum 14X                           Eugenia Jambosa 7X                                 Sarsparilla 10X

Arnica Montana Radix 8X                            Eupatorium Perfoliatum 10X                      Terebinthina 14X, 20X

Arsenicum Iodatum 14X                              Faxinus Americana 7X                               Teucrium Marum 6X

Baptisia Tinc 10X                                        Hyoscyamus Nig Tinc 7X                             Thlaspi Bursa Pastorius 10X

Benzinum 12X                                            Ledum Palustre 10X                                   Vibrunum Opulus 15X

Cobaltum Metallicum 14X                           Leptandra Virginica 10X, 15X

Crataegus Oxyacantha 10X                       Nicotinum 9X, 12X

L-Trans

INACTIVE INGREDIENT SECTION

Alcohol, Purified Water

L-Trans

WARNINGS SECTION

Use only under the direction of a health care professional. Do not use if tamper evident seal is broken or missing.

L-Trans

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

L-Trans

INDICATIONS & USAGE SECTION

For the temporary relief of swelling, bloating, tinnitus, dizziness, nausea, head and neck pain, and muscle spasms.

L-Trans

DOSAGE & ADMINISTRATION SECTION

Orally 25 drops, 2 times per day or as indicated by a physician. Children 12 and under use one half the adult dosage.

L-Trans

OTC - PURPOSE SECTION

Aids movement and vitality within the lymphatic system.

L-Trans

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
dbebfdf8-6e0c-cfa8-fdbc-e5d7f1bf1562Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64616-095-02L-Trans59 mL in 1 BOTTLE, DROPPERLIQUID598

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARNICA MONTANAACTIVE INGREDIENTO80TY208ZW1
ARSENIC TRIIODIDEACTIVE INGREDIENT3029988O2T1
BAPTISIA TINCTORIAACTIVE INGREDIENT5K1UO2888Y1
BENZENEACTIVE INGREDIENTJ64922108F1
CAPSELLA BURSA-PASTORISACTIVE INGREDIENTW0X9457M591
COBALTACTIVE INGREDIENT3G0H8C93621
CRATAEGUS FRUITACTIVE INGREDIENTQ21UUL21051
EUPATORIUM PERFOLIATUM FLOWERING TOPACTIVE INGREDIENT1W0775VX6E1
FRAXINUS AMERICANA BARKACTIVE INGREDIENT0B24UR1O1S1
HYOSCYAMUS NIGERACTIVE INGREDIENT4WRK2153H31
LEDUM PALUSTRE TWIGACTIVE INGREDIENT877L01IZ0P1
NICOTINEACTIVE INGREDIENT6M3C89ZY6R1
SARSAPARILLAACTIVE INGREDIENT2H1576D5WG1
SILVERACTIVE INGREDIENT3M4G523W1G1
SYZYGIUM JAMBOS SEEDACTIVE INGREDIENT97P0H458691
TEUCRIUM MARUMACTIVE INGREDIENT10464S0TAA1
TURPENTINE OILACTIVE INGREDIENTC5H0QJ6V7F1
VERONICASTRUM VIRGINICUM ROOTACTIVE INGREDIENTM2O62YTN421
VIBURNUM OPULUS BARKACTIVE INGREDIENTT1UG6H68051
ARNICA MONTANAACTIVE MOIETYO80TY208ZW1
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
BAPTISIA TINCTORIAACTIVE MOIETY5K1UO2888Y1
BENZENEACTIVE MOIETYJ64922108F1
CAPSELLA BURSA-PASTORISACTIVE MOIETYW0X9457M591
COBALTACTIVE MOIETY3G0H8C93621
CRATAEGUS FRUITACTIVE MOIETYQ21UUL21051
CULVER'S ROOTACTIVE MOIETYM2O62YTN421
EUPATORIUM PERFOLIATUM FLOWERING TOPACTIVE MOIETY1W0775VX6E1
FRAXINUS AMERICANA BARKACTIVE MOIETY0B24UR1O1S1
HYOSCYAMUS NIGERACTIVE MOIETY4WRK2153H31
LEDUM PALUSTRE TWIGACTIVE MOIETY877L01IZ0P1
NICOTINEACTIVE MOIETY6M3C89ZY6R1
SARSAPARILLAACTIVE MOIETY2H1576D5WG1
SILVERACTIVE MOIETY3M4G523W1G1
SYZYGIUM JAMBOS SEEDACTIVE MOIETY97P0H458691
TEUCRIUM MARUMACTIVE MOIETY10464S0TAA1
TURPENTINE OILACTIVE MOIETYC5H0QJ6V7F1
VIBURNUM OPULUS BARKACTIVE MOIETYT1UG6H68051
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64616-09564616-095-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
L-TransLYMPH SYSTEM BOOSTERVitality Works, Inc.72ccb9be-2d62-414a-856a-7fcea51f26d22025-12-17WarningsExact identifier
ndc (package): 64616-095-02
ndc (product): 64616-095
ndc11 (package): 64616009502
spl id: 462f54f9-4506-d643-e063-6394a90ab1d5
spl set id: 72ccb9be-2d62-414a-856a-7fcea51f26d2

Reported adverse events (FAERS/openFDA)#

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