NDC 43406-0128 Animal Antigen

Feliscatushair, Bostaurushair, Bostaurusskin, Gallusgallusfeather, Canislupusfamiliarisskin, Canisfamiliarishair, Anasplatyrhynchosfeather, Anseranserfeather, Caviaporcellushair, Caviaporcellusskin, Mesocricetusauratushair, Mesocricetusauratusskin, Susscrofahair, Susscrofaskin, Equuscaballushair, Equuscaballusdander, Musmusculushair, Musmusculuasskin, Oryctolaguscuniculusskin, Oryctolaguscuniculushair, Ovisarieswhole, Meleagrisgallopavofeather, Arsenictrioxide, Blattaorientalis, Strychnosnux-vomicaseed, Phosphorus, Pulsatilla, Sulfur Liquid Oral

  1. Labeler Index
  2. Natural Creations, Inc.
  3. NDC: 43406-0128 Animal Antigen

NDC Product Code 43406-0128

NDC CODE: 43406-0128

Proprietary Name: Animal Antigen 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: Feliscatushair, Bostaurushair, Bostaurusskin, Gallusgallusfeather, Canislupusfamiliarisskin, Canisfamiliarishair, Anasplatyrhynchosfeather, Anseranserfeather, Caviaporcellushair, Caviaporcellusskin, Mesocricetusauratushair, Mesocricetusauratusskin, Susscrofahair, Susscrofaskin, Equuscaballushair, Equuscaballusdander, Musmusculushair, Musmusculuasskin, Oryctolaguscuniculusskin, Oryctolaguscuniculushair, Ovisarieswhole, Meleagrisgallopavofeather, Arsenictrioxide, Blattaorientalis, Strychnosnux-vomicaseed, Phosphorus, Pulsatilla, 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.
  • This product is used as uses:  temporarily relieves symptoms associated with allergic responses to animals.**

NDC Code Structure

NDC 43406-0128-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Animal Antigen with NDC 43406-0128 is a human prescription drug product labeled by Natural Creations, Inc.. The generic name of Animal Antigen is feliscatushair, bostaurushair, bostaurusskin, gallusgallusfeather, canislupusfamiliarisskin, canisfamiliarishair, anasplatyrhynchosfeather, anseranserfeather, caviaporcellushair, caviaporcellusskin, mesocricetusauratushair, mesocricetusauratusskin, susscrofahair, susscrofaskin, equuscaballushair, equuscaballusdander, musmusculushair, musmusculuasskin, oryctolaguscuniculusskin, oryctolaguscuniculushair, ovisarieswhole, meleagrisgallopavofeather, arsenictrioxide, blattaorientalis, strychnosnux-vomicaseed, phosphorus, pulsatilla, sulfur. The product's dosage form is liquid and is administered via oral form.

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 Prescription 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.

Animal Antigen 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.

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.

Pharmacologic Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Product Labeler Information

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

Labeler Name: Natural Creations, Inc.
Labeler Code: 43406
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: 05-29-2007 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: 12-31-2023 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Animal Antigen Product Label Images

Animal Antigen 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 INGREDIENTS:  Cat* 12X, 15X, 30X, Cattle** 12X, 15X, 30X, Chicken*** 12X, 15X, 30X,  Dog** 12X, 15X, 30X, Duck*** 12X, 15X, 30X,  Goose*** 12X, 15X, 30X, Guinea Pig** 12X, 15X, 30X, Hamster** 12X, 15X, 30X, Hog**12X, 15X, 30X, Horse**** 12X, 15X, 30X, Mouse** 12X, 15X, 30X, Rabbit** 12X, 15X, 30X, Sheep 12X, 15X, 30X, Turkey*** 12X, 15X, 30X, Arsenicum Album 30C, Blata Orientalis 30C, Nux Vomica 30C, Phosphorus 30C, Pulsatilla 30C, Sulphur 30C.*Hair, **Hair & Epithelia, ***Feathers, ****Hair & Dander.

Otc - Purpose

Uses:  Temporarily relieves symptoms associated with allergic responses to animals.**

Indications & Usage

Uses:  Temporarily relieves symptoms associated with allergic responses to animals.

Dosage & Administration

Directions:  Adults & children above 12 years:  10 drops orally 3 times daily, or as directed by a health care professional.

Otc - Keep Out Of Reach Of Children

  • WARNINGS:Consult a physician for use in children under 12 years of age.IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.KEEP OUT OF THE REACH OF CHILDREN.  In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.Do not use if TAMPER EVIDENT seal is broken or missing.

Warnings

  • WARNINGS:Consult a physician for use in children under 12 years of age.IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.Do not use if TAMPER EVIDENT seal is broken or missing.

Inactive Ingredient

Inactive Ingredients:  Purified Water, Ethyl Alcohol USP.

Otc - Questions

Questions & Comments?Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

References

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

* Please review the disclaimer below.