RPT-Sys

Manufacturer
Vitality Works, Inc. | Vitality Works, Inc
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:03

Label at a glance#

ProductRPT-Sys
Active ingredientTOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, THYROID, UNSPECIFIED, TRILLIUM ERECTUM ROOT, APOCYNUM CANNABINUM ROOT, ASAFETIDA, SODIUM BORATE, EUCALYPTUS GLOBULUS LEAF, GENTIANA LUTEA ROOT, STRYCHNOS IGNATII SEED, WOOD CREOSOTE, LATHYRUS SATIVAS SEED, EGG PHOSPHOLIPIDS, LYCOPODIUM CLAVATUM SPORE, NUTMEG, OXALIC ACID DIHYDRATE, PHOSPHORIC ACID, SUS SCROFA PITUITARY GLAND, PLATINUM
Label structure8 sections

Label contents#

Full prescribing information#

RPT-Sys

OTC - ACTIVE INGREDIENT SECTION

Apocynum Cannabinum 10X                     Lathyrus Sativus 10X, 20X                      Plantinum Metallicum 10X

Asafoetida 6X                                           Lecithin 10X, 20X                                    Rhus Toxicodendron 5X, 10X

Borax 7X                                                   Lycopodium Clavatum 7X                       Silicea 10X

Eucalyptus Globulus 7X                            Nux Moschata 7X                                    Thyroidinum 6C

Gentiana Lutea 7X                                   Oxalicum Acidum 10X                              Trillum Pendulum 3X

Ignatia Amara 5X, 10X                             Phophoricum Acidum 8X

Kreosotum 8X                                          Pituitarum Posterium 6C

RPT-Sys

INACTIVE INGREDIENT SECTION

Alcohol, Purified Water

RPT-Sys

WARNINGS SECTION

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

RPT-Sys

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.

RPT-Sys

INDICATIONS & USAGE SECTION

For the temporary relief of anxiety, confusion, memory loss, and depression.

RPT-Sys

DOSAGE & ADMINISTRATION SECTION

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

RPT-Sys

OTC - PURPOSE SECTION

Focuses on the vibrational and electrical balances to the body.

RPT-Sys

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64616-104-02RPT-Sys59 mL in 1 BOTTLE, DROPPERLIQUID598

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APOCYNUM CANNABINUM ROOTACTIVE INGREDIENT2F92409L9Z1
ASAFETIDAACTIVE INGREDIENTW9FZA51AS11
EGG PHOSPHOLIPIDSACTIVE INGREDIENT1Z74184RGV1
EUCALYPTUS GLOBULUS LEAFACTIVE INGREDIENTS546YLW6E61
GENTIANA LUTEA ROOTACTIVE INGREDIENTS72O3284MS1
LATHYRUS SATIVAS SEEDACTIVE INGREDIENT8VP54WOT4I1
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
NUTMEGACTIVE INGREDIENTAEE24M3MQ91
OXALIC ACID DIHYDRATEACTIVE INGREDIENT0K2L2IJ59O1
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
PLATINUMACTIVE INGREDIENT49DFR088MY1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
Sodium BorateACTIVE INGREDIENT91MBZ8H3QO1
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
SUS SCROFA PITUITARY GLANDACTIVE INGREDIENTE8S87O660T1
THYROID, UNSPECIFIEDACTIVE INGREDIENT0B4FDL9I6P1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A1
TRILLIUM ERECTUM ROOTACTIVE INGREDIENTAHW6F0T2X01
WOOD CREOSOTEACTIVE INGREDIENT3JYG22FD731
APOCYNUM CANNABINUM ROOTACTIVE MOIETY2F92409L9Z1
ASAFETIDAACTIVE MOIETYW9FZA51AS11
BORATE IONACTIVE MOIETY44OAE30D221
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
EGG PHOSPHOLIPIDSACTIVE MOIETY1Z74184RGV1
EUCALYPTUS GLOBULUS LEAFACTIVE MOIETYS546YLW6E61
GENTIANA LUTEA ROOTACTIVE MOIETYS72O3284MS1
LATHYRUS SATIVAS SEEDACTIVE MOIETY8VP54WOT4I1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
NUTMEGACTIVE MOIETYAEE24M3MQ91
OXALIC ACIDACTIVE MOIETY9E7R5L6H311
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
PLATINUMACTIVE MOIETY49DFR088MY1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
SUS SCROFA PITUITARY GLANDACTIVE MOIETYE8S87O660T1
THYROID, UNSPECIFIEDACTIVE MOIETY0B4FDL9I6P1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A1
TRILLIUM ERECTUM ROOTACTIVE MOIETYAHW6F0T2X01
WOOD CREOSOTEACTIVE MOIETY3JYG22FD731
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
64616-10464616-104-02

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
RPT-SysEMOTIONAL REBALANCEVitality Works, Inc.0e8768fe-c2ba-41e9-93ac-c142fae6e8792025-12-17WarningsExact identifier
ndc (package): 64616-104-02
ndc (product): 64616-104
ndc11 (package): 64616010402
spl id: 462f5aa4-db68-26dd-e063-6294a90a4030
spl set id: 0e8768fe-c2ba-41e9-93ac-c142fae6e879

Reported adverse events (FAERS/openFDA)#

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