What is NDC 61096-2030?

61096-2030 is the product NDC for Party Relief, Arsenic trioxide 200 [hp_C]/41mL + 12 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Party Relief (Arsenicum alb, Avena, Bryonia, Capsicum, Carbo an, Carduus mar, Chelidonium maj, Hepar suis, Kali iod, Lapis, Radium brom, Taraxacum, Thuja occ).

What is the active ingredient?

Arsenic 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.

Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Party Relief?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Party Relief NDC 61096-2030 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61096-2030Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61096-2030Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
61096-2030-1	6109620300161096203001	1 BOTTLE, SPRAY in 1 CARTON (61096-2030-1) / 41 mL in 1 BOTTLE, SPRAYMarketed from Mar 12, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Party Relief
Generic name (nonproprietary): arsenicum alb, avena, bryonia, capsicum, carbo an, carduus mar, chelidonium maj, hepar suis, kali iod, lapis, radium brom, taraxacum, thuja occ
Active ingredients: Arsenic trioxide — 200 [hp_C]/41mLAvena sativa flowering top — 4 [hp_X]/41mLBryonia alba root — 200 [hp_C]/41mLCapsicum — 6 [hp_X]/41mLCarbo animalis — 200 [hp_C]/41mLMilk thistle — 4 [hp_X]/41mLChelidonium majus whole — 200 [hp_C]/41mLPork liver — 6 [hp_X]/41mLPotassium iodide — 200 [hp_C]/41mLCalcium hexafluorosilicate — 200 [hp_C]/41mLRadium bromide — 200 [hp_C]/41mLTaraxacum officinale — 4 [hp_X]/41mLThuja occidentalis leafy twig — 200 [hp_C]/41mL
Dosage form: Liquid
Route: Oral
Labeler: Eight and Company L.L.CNDC labeler code 61096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 12, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 61096-2030_9348e742-f0a1-4cb0-a745-1026c6205351SPL ID 9348e742-f0a1-4cb0-a745-1026c6205351SPL set ID efadeae2-1ed9-4e80-9909-908bde98965bUNII S7V92P67HO, MA9CQJ3F7F, T7J046YI2B, 00UK7646FG, 279O8I0433, U946SH95EE, 7E889U5RNN, 6EC706HI7F, 1C4QK22F9J, 2NVP93XVQ3, R74O7T8569, 39981FM375, 1NT28V9397
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461096203001 followed by a unit qualifier and the quantity

Package 61096-2030-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 18, 2025.

Indications (excerpt from the label)

INDICATIONS: 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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61096-2030

What is NDC 61096-2030?: 61096-2030 is the product NDC for Party Relief, Arsenic trioxide 200 [hp_C]/41mL + 12 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Party Relief (Arsenicum alb, Avena, Bryonia, Capsicum, Carbo an, Carduus mar, Chelidonium maj, Hepar suis, Kali iod, Lapis, Radium brom, Taraxacum, Thuja occ).
What is the active ingredient?: Arsenic 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.
Who is the labeler?: Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Party Relief?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.