NDC 73092-0001 Oxyhives

Apis Mellifica, Arnica Montana, Hepar Suis, Ichthyolum, Lachesis Mutus, Mercurius Solubilis, Rhus Tox, Urtica Urens

NDC Product Code 73092-0001

NDC Code: 73092-0001

Proprietary Name: Oxyhives 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: Apis Mellifica, Arnica Montana, Hepar Suis, Ichthyolum, Lachesis Mutus, Mercurius Solubilis, Rhus Tox, Urtica Urens 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

  • 73092 - Publisher Payments, Llc

NDC 73092-0001-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Oxyhives with NDC 73092-0001 is a a human over the counter drug product labeled by Publisher Payments, Llc. The generic name of Oxyhives is apis mellifica, arnica montana, hepar suis, ichthyolum, lachesis mutus, mercurius solubilis, rhus tox, urtica urens. The product's dosage form is spray and is administered via oral form.

Labeler Name: Publisher Payments, Llc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Oxyhives 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.

  • APIS MELLIFERA 200 [hp_C]/mL
  • ARNICA MONTANA 6 [hp_X]/mL
  • PORK LIVER 6 [hp_X]/mL
  • ICHTHAMMOL 6 [hp_X]/mL
  • URTICA URENS 200 [hp_C]/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

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: Publisher Payments, Llc
Labeler Code: 73092
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: 05-24-2019 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.

Oxyhives Product Label Images

Oxyhives 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

Active Ingredients:

Apis Mellifica 200C, Arnica Montana 6X, Hepar Suis 6X, Ichthyolum 6X, Lachesis Mutus 30C, Mercurius Solubilis 200C, Rhus Tox 200C, Urtica Urens 200C.


Relieves symptoms associated with Hives.

Relieves symptoms associated with Hives.


If you are pregnant or breast-feeding, seek the advice of a doctor before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.DO Not use if TAMPER EVIDENT seal around the neck of the bottle is missing or broken.

Keep Out Of Reach Of Children:

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


Adults and children over 12, spray twice under the tongue three times per day.For children under 12, consult a doctor prior to use.

Inactive Ingredients:

Alcohol 20% v/v, Purified water.


Distributed By: Publisher Payments, LLCPO Box 7574 Milton Keynes, MK119GQ, United KingdomMon/Fri 9AM to 5PM PST 1-800-756-4120

Package Label Display:

OxyHivesHives ReliefHOMEOPATHIC1.0 FL OZ. (30 ml)

* Please review the disclaimer below.