FDA.reportPublic FDA data

Slenderiix

Manufacturer
Vitality Works | Vitality Works Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:07

Label at a glance#

ProductSlenderiix
Active ingredientSULFURIC ACID, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LYCOPODIUM CLAVATUM SPORE, AMMONIUM BROMIDE, STRYCHNOS NUX-VOMICA SEED, AVENA SATIVA FLOWERING TOP, GRAPHITE, THYROID, UNSPECIFIED, STRYCHNOS IGNATII SEED, FUCUS VESICULOSUS
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonium Bromatum 12X

Avena Sativa 6X

Calcarea Carbomica 6x

Focus Vesiculous 6X

Graphites 12 X

Ignata Amara 6X

Lycopodium Clavatum 6X

Nux Vomica 6X

Sulfuricum Acidum 6X

Thyroiinum 6X

INACTIVE INGREDIENT SECTION

Grain Alcohol (20% by volume), Natural Flavors, Stevia Leaf, USP Purified Water

WARNINGS SECTION

If pregnant or breast-feeding, do not use. Not for use by children under 18.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Helps to temporarily reduce minor hunger pangs and control appetite to support weight loss efforts

DOSAGE & ADMINISTRATION SECTION

Adults place 10-15 drops under the tongue three times per day. Leave uner tongue for 10 seconds, then swallow. Do Not eat or drink 10 minutes before or after taking the drops.

OTC - PURPOSE SECTION

Weight Management formula

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Slenderiix labelSlenderiix label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64616-077-012023-12-29C16284748780-1f386c649-e6ac-0266-e053-dadaa90a7c1aSlenderiix
64616-077-012023-01-30C16284748780-1f386c649-e6ac-0266-e053-dadaa90a7c1aSlenderiix

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64616-077-01Slenderiix59 mL in 1 BOTTLE, DROPPERLIQUID598

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMMONIUM BROMIDEACTIVE INGREDIENTR0JB3224WS1
AVENA SATIVA FLOWERING TOPACTIVE INGREDIENTMA9CQJ3F7F1
FUCUS VESICULOSUSACTIVE INGREDIENT535G2ABX9M1
GRAPHITEACTIVE INGREDIENT4QQN74LH4O1
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
SULFURIC ACIDACTIVE INGREDIENTO40UQP6WCF1
THYROID, UNSPECIFIEDACTIVE INGREDIENT0B4FDL9I6P1
AVENA SATIVA FLOWERING TOPACTIVE MOIETYMA9CQJ3F7F1
BROMIDE IONACTIVE MOIETY952902IX061
FUCUS VESICULOSUSACTIVE MOIETY535G2ABX9M1
GRAPHITEACTIVE MOIETY4QQN74LH4O1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487K1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
SULFURIC ACIDACTIVE MOIETYO40UQP6WCF1
THYROID, UNSPECIFIEDACTIVE MOIETY0B4FDL9I6P1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V31
STEVIA LEAFINACTIVE INGREDIENT6TC6NN08761
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64616-07764616-077-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFURIC ACIDO40UQP6WCFACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
AMMONIUM BROMIDER0JB3224WSACTIB
ALCOHOL3K9958V90MIACT
PEPPERMINT OILAV092KU4JHIACT
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
AVENA SATIVA FLOWERING TOPMA9CQJ3F7FACTIB
GRAPHITE4QQN74LH4OACTIB
STEVIA LEAF6TC6NN0876IACT
THYROID, UNSPECIFIED0B4FDL9I6PACTIB
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
FUCUS VESICULOSUS535G2ABX9MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT

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 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3LIQUID / ORAL29008 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
PROPYLENE GLYCOLPROPYLENE GLYCOL6DC9Q167V3LIQUID / ORAL29008 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 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
SlenderiixWEIGHT MANAGEMENT FORMULAVitality Works398251ec-6834-4dda-abc6-f503632d16322025-12-17WarningsExact identifier
ndc (package): 64616-077-01
ndc (product): 64616-077
ndc11 (package): 64616007701
spl id: 462f70d9-439e-e6b2-e063-6394a90a1bbb
spl set id: 398251ec-6834-4dda-abc6-f503632d1632

Reported adverse events (FAERS/openFDA)#

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