NDC 54973-4007 Quitters Relief Irritability

Aconitum Napellus Whole, Anamirta Cocculus Seed, Arsenic Trioxide, Delphinium Staphisagria Seed, Dibasic Potassium Phosphate, Gelsemium Sempervirens Root, Phosphorus, Silver Nitrate And Sulfur

NDC Product Code 54973-4007

NDC CODE: 54973-4007

Proprietary Name: Quitters Relief Irritability 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: Aconitum Napellus Whole, Anamirta Cocculus Seed, Arsenic Trioxide, Delphinium Staphisagria Seed, Dibasic Potassium Phosphate, Gelsemium Sempervirens Root, Phosphorus, Silver Nitrate And Sulfur 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).

Product Characteristics

Shape: ROUND (C48348)
9 MM
Score: 1

NDC Code Structure

  • 54973 - Hyland's

NDC 54973-4007-1

Package Description: 1 BOTTLE in 1 CARTON > 100 TABLET in 1 BOTTLE

NDC Product Information

Quitters Relief Irritability with NDC 54973-4007 is a a human over the counter drug product labeled by Hyland's. The generic name of Quitters Relief Irritability is aconitum napellus whole, anamirta cocculus seed, arsenic trioxide, delphinium staphisagria seed, dibasic potassium phosphate, gelsemium sempervirens root, phosphorus, silver nitrate and sulfur. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Hyland's

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

Quitters Relief Irritability 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.

  • SILVER NITRATE 30 [hp_X]/1
  • SULFUR 30 [hp_X]/1
  • ARSENIC TRIOXIDE 30 [hp_X]/1
  • PHOSPHORUS 30 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ACACIA (UNII: 5C5403N26O)

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: Hyland's
Labeler Code: 54973
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: 12-15-2020 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: 12-31-2021 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.

Quitters Relief Irritability Product Label Images

Quitters Relief Irritability 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 - Purpose

Temporarily relieves symptoms of irritability associated with smoking cessation, including: anxiousness, restlessness, nervous, tension, occasional sleeplessness

Active Ingredients

Active ingredientsPurposeAconitum Napellus 30X HPUSnervous tensionArgentum Nitricum 30X HPUSnervous tensionArsenicum Album 30X HPUSnervousness, restlessness, anxiousnessCocculus Indicus 30X HPUSanxiousness, restlessnessGelsemium Sempervirens 30X HPUSirritabilityIgnatia Amara 30X HPUS(less than 0.0000000000017% Alkaloids, calculated)anxiousness, occasional sleeplessnessKali Phosphoricum 12X HPUSirritabilityPhosphorus 30X HPUSoccasional sleeplessnessStaphysagria 12X HPUSanxiousness and irritability associated with smoking cessationSulphur 30X HPUSirritability


"HPUS" indicates that the active ingredients are in the official Homeopathic Pharmacopoeia of the United States.



■ Temporarily relieves symptoms of irritability associated with smoking cessation, including:■ anxiousness ■ restlessness ■ nervous tension ■ occasional sleeplessness

Otc - Pregnancy Or Breast Feeding

As with any drug, ask a doctor before use if pregnant or breast-feeding.

Otc - Do Not Use

Do not use more than directed.

Otc - Ask Doctor

Consult a physician if symptoms persist for more than 7 days or worsen.

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of the reach of children.


In case of emergency or accidental overdose, contact a medical professional or Poison Control Center immediately. Hyland’s may also be contacted for emergency information about our products 24 hours a day, 7 days per week at (800) 624-9659.


Adults ages 18years and overDissolve 2 tablets under tongue every 15 minutes up to 4 doses,then every 4 hours until relieved.

Other Information

■ Do not use if imprinted "SEALED FOR YOUR PROTECTION" tamper-evident bottle cap band is broken or missing.

Inactive Ingredients

Acacia Gum, Lactose.

* Please review the disclaimer below.