43406-0002 NDC - ALLERGY HP (ONION, AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, ACTIVATED CHARCOAL, EUPHRASIA STRICTA, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, SOLIDAGO VIRGAUREA FLOWERING TOP, SULFUR)

Drug Information

  • Product NDC: 43406-0002
  • Proprietary Name: Allergy HP
  • Non Proprietary Name: Onion, Ambrosia Artemisiifolia, Arsenic Trioxide, Activated Charcoal, Euphrasia Stricta, Strychnos Nux-Vomica Seed, Pulsatilla Vulgaris, Solidago Virgaurea Flowering Top, Sulfur
  • Active Ingredient(s): 30 [hp_C]/mL ACTIVATED CHARCOAL; 30 [hp_C]/mL AMBROSIA ARTEMISIIFOLIA; 30 [hp_C]/mL ARSENIC TRIOXIDE; 30 [hp_C]/mL EUPHRASIA STRICTA; 30 [hp_C]/mL ONION; 30 [hp_C]/mL PULSATILLA VULGARIS; 30 [hp_C]/mL SOLIDAGO VIRGAUREA FLOWERING TOP; 30 [hp_C]/mL STRYCHNOS NUX-VOMICA SEED; 30 [hp_C]/mL SULFUR
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Natural Creations, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/29/2007

Package Information

No. Package Code Package Description Billing Unit
143406-0002-130 mL in 1 BOTTLE, DROPPER (43406-0002-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43406-0002The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEAllergy HPThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEOnion, Ambrosia Artemisiifolia, Arsenic Trioxide, Activated Charcoal, Euphrasia Stricta, Strychnos Nux-Vomica Seed, Pulsatilla Vulgaris, Solidago Virgaurea Flowering Top, SulfurThis is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
DOSAGE FORM NAMELIQUIDProduct 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.
ROUTE NAMEORALThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
START MARKETING DATE5/29/2007Name of Company corresponding to the labeler code segment of the Product NDC.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMENatural Creations, Inc.The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; AMBROSIA ARTEMISIIFOLIA; ARSENIC TRIOXIDE; EUPHRASIA STRICTA; ONION; PULSATILLA VULGARIS; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; SULFURAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH30; 30; 30; 30; 30; 30; 30; 30; 30 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS] 

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This page was last updated on: 11/21/2025

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