Party Relief

Manufacturer
Eight and Company L.L.C | King Bio Inc. | Apotheca Company
Effective date
2025-12-18
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:36:21

Label at a glance#

ProductParty Relief
Active ingredientARSENIC TRIOXIDE, AVENA SATIVA FLOWERING TOP, BRYONIA ALBA ROOT, CAPSICUM, CARBO ANIMALIS, MILK THISTLE, CHELIDONIUM MAJUS WHOLE, PORK LIVER, POTASSIUM IODIDE, CALCIUM HEXAFLUOROSILICATE, RADIUM BROMIDE, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Dosage and administration

Adults Only. For Prevention: Spray 2 times into the mouth prior to drinking alcoholic beverages, after each hour of drinking and when alcohol consumption has ended. For relief the day after: spray 2 sprays into the mouth as needed up to 6 times a day.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Arsenicum Album 200C, Avena Sativa 4X, Bryonia (Alba) 200C, Capsicum  Annuum 6X, Carbo Animalis 200C, Carduus Marianus 4X, Chelidonium Majus 200C, Hepar Suis 6X, Kali Iodatum 200C, Lapis Albus 200C, Radium Bromatum 200C, Taraxacum Officinale 4X, Thuja Occidentalis 200C.

PURPOSE:

OTC - PURPOSE SECTION

Temporarily relieves the symptoms of alcohol-related discomfort including:

° headache and dehydration

° upset stomach/nausea

° sluggish feeling

° liver toxicity

WARNINGS:

WARNINGS SECTION

If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults Only. For Prevention: Spray 2 times into the mouth prior to drinking alcoholic beverages, after each hour of drinking and when alcohol consumption has ended.
For relief the day after: spray 2 sprays into the mouth as needed up to 6 times a day.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Do not use if the transparent seal around spray bottle is broken or missing.

INDICATIONS:

INDICATIONS & USAGE SECTION

Temporarily relieves the symptoms of alcohol-related discomfort including:

° headache and dehydration

° upset stomach/nausea

° sluggish feeling

° liver toxicity

° natural

° gluten & lactose free

° no artifical flavors or colors

° no known negative side effects

° no known negative drug interactions

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Non-GMO Glycerin, organic alcohol 20% v/v, purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

Manufactured for Eight and Company L.L.C.

Gaithersburg, MD 20879 1.800.377.5787

www.sprayology.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61096-2030-1

sprayology

Party Relief

PREVENTS + RELIEVES HANGOVERS

HOMEOPATHIC ORAL SPRAY W/ MILK THISTLE

[drink responsibly, this product does not prevent alcohol intoxication]

1.38 fl.oz (41 ml)

Party Relief LBLParty Relief LBL

Party Relief CNTParty Relief CNT

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130361096003017GTIN-13: 0361096003017
EAN-13: 0361096003017
GTIN-12: 361096003017
UPC-A: 361096003017
GTIN storage (14 digits): 00361096003017
ETCO0013 Party Relief CTN 9-27-21.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61096-2030-12023-12-01C16284748780-1ba0f9c33-10fb-a910-e053-dadaa90a0b85Party Relief
61096-2030-12023-01-30C16284748780-1ba0f9c33-10fb-a910-e053-dadaa90a0b85Party Relief
61096-2030-12021-02-16C16284748780-1ba0f9c33-10fb-a910-e053-dadaa90a0b85Party Relief
61096-2030-12021-01-29C16284748780-1ba0f9c33-10fb-a910-e053-dadaa90a0b85Party Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61096-2030-1Party Relief41 mL in 1 BOTTLE, SPRAYLIQUID418
61096-2030-1Party Relief1 in 1 CARTONLIQUID18

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
AVENA SATIVA FLOWERING TOPACTIVE INGREDIENTMA9CQJ3F7F1
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B1
CALCIUM HEXAFLUOROSILICATEACTIVE INGREDIENT2NVP93XVQ31
CAPSICUMACTIVE INGREDIENT00UK7646FG1
CARBO ANIMALISACTIVE INGREDIENT279O8I04331
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNN1
MILK THISTLEACTIVE INGREDIENTU946SH95EE1
PORK LIVERACTIVE INGREDIENT6EC706HI7F1
POTASSIUM IODIDEACTIVE INGREDIENT1C4QK22F9J1
RADIUM BROMIDEACTIVE INGREDIENTR74O7T85691
TARAXACUM OFFICINALEACTIVE INGREDIENT39981FM3751
THUJA OCCIDENTALIS LEAFY TWIGACTIVE INGREDIENT1NT28V93971
ARSENIC CATION (3+)ACTIVE MOIETYC96613F5AV1
AVENA SATIVA FLOWERING TOPACTIVE MOIETYMA9CQJ3F7F1
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B1
CALCIUM HEXAFLUOROSILICATEACTIVE MOIETY2NVP93XVQ31
CAPSICUMACTIVE MOIETY00UK7646FG1
CARBO ANIMALISACTIVE MOIETY279O8I04331
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNN1
IODIDE IONACTIVE MOIETY09G4I6V86Q1
MILK THISTLEACTIVE MOIETYU946SH95EE1
PORK LIVERACTIVE MOIETY6EC706HI7F1
RADIUM CATIONACTIVE MOIETY05456MVL7T1
TARAXACUM OFFICINALEACTIVE MOIETY39981FM3751
THUJA OCCIDENTALIS LEAFY TWIGACTIVE MOIETY1NT28V93971
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61096-203061096-2030-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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 · 4 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
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
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
Party ReliefARSENICUM ALB, AVENA, BRYONIA, CAPSICUM, CARBO AN, CARDUUS MAR, CHELIDONIUM MAJ, HEPAR SUIS, KALI IOD, LAPIS, RADIUM BROM, TARAXACUM, THUJA OCCEight and Company L.L.Cefadeae2-1ed9-4e80-9909-908bde98965b2025-12-18WarningsExact identifier
ndc (package): 61096-2030-1
ndc (product): 61096-2030
ndc11 (package): 61096203001
spl id: 9348e742-f0a1-4cb0-a745-1026c6205351
spl set id: efadeae2-1ed9-4e80-9909-908bde98965b

Reported adverse events (FAERS/openFDA)#

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