NDC 61096-2030 Party Relief

Arsenicum Alb, Avena, Bryonia, Capsicum, Carbo An, Carduus Mar, Chelidonium Maj, Hepar Suis, Kali Iod, Lapis, Radium Brom, Taraxacum, Thuja Occ

NDC Product Code 61096-2030

NDC Code: 61096-2030

Proprietary Name: Party Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Arsenicum Alb, Avena, Bryonia, Capsicum, Carbo An, Carduus Mar, Chelidonium Maj, Hepar Suis, Kali Iod, Lapis, Radium Brom, Taraxacum, Thuja Occ What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 61096 - Eight And Company L.l.c
    • 61096-2030 - Party Relief

NDC 61096-2030-1

Package Description: 1 BOTTLE, SPRAY in 1 CARTON > 41 mL in 1 BOTTLE, SPRAY

NDC Product Information

Party Relief with NDC 61096-2030 is a a human over the counter drug product labeled by Eight And Company L.l.c. The generic name of Party Relief is arsenicum alb, avena, bryonia, capsicum, carbo an, carduus mar, chelidonium maj, hepar suis, kali iod, lapis, radium brom, taraxacum, thuja occ. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Eight And Company L.l.c

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Party Relief Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARSENIC TRIOXIDE 200 [hp_C]/41mL
  • BRYONIA ALBA ROOT 200 [hp_C]/41mL
  • CAPSICUM 6 [hp_X]/41mL
  • CARBO ANIMALIS 200 [hp_C]/41mL
  • MILK THISTLE 4 [hp_X]/41mL
  • CHELIDONIUM MAJUS 200 [hp_C]/41mL
  • PORK LIVER 6 [hp_X]/41mL
  • POTASSIUM IODIDE 200 [hp_C]/41mL
  • RADIUM BROMIDE 200 [hp_C]/41mL

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Eight And Company L.l.c
Labeler Code: 61096
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-12-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Party Relief Product Label Images

Party Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredient: Arsenicum album 200C, Avena sativa 1X, Bryonia 200C, Capsicum annuum 6X, Carbo animalis 200C, Carduus marianus 1X, Chelidonium majus 200C, Hepar suis 6X, Kali iodatum 200C, Lapis albus 200C, Radium bromatum 200C, Taraxacum officinale 1X, Thuja occidentalis 200C.


Warnings: 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.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Purpose

  • Temporarily relieves the symptoms of alcohol-related discomfort including:headache and dehydration upset stomach/nauseasluggish feelingliver toxicity

Dosage & Administration

  • Directions: 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 Safety Information

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

Inactive Ingredient

Inactive Ingredients: Glycerin 10%, v/v, non-GMO organic alcohol 9% v/v, purified water.

Indications & Usage

Temporarily relieves the symptoms of alcohol-related discomfort including:° headache and dehydration° upset stomach/nausea° sluggish feeling° liver toxicity° natural° gluten free° no artifical flavors or colors° no known negative side effects° no known negative drug interactions

* Please review the disclaimer below.

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