NDC 43406-0106

ALLERGY NEW ENGLAND MIX

Betula Pubescens Bark, Artemisia Vulgaris Pollen, Plantago Lanceolata Pollen, Acer Pseudoplatanus Pollen, Betula Pubescens Bark, Evernia Prunastri Bark, Armaranthus Retroflexus Pollen, Pinus Massoniana Pollen, Tabuliformis Pollen, Ambrosia Artemisifolia Pollen,

ALLERGY NEW ENGLAND MIX is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Natural Creations, Inc.. The primary component is Betula Pubescens Bark; Artemisia Vulgaris Pollen; Plantago Lanceolata Pollen; Acer Pseudoplatanus Pollen; Evernia Prunastri; Amaranthus Retroflexus Pollen; Pinus Massoniana Pollen; Pinus Tabuliformis Pollen; Ambrosia Artemisiifolia Pollen; Juniperus Virginiana Pollen; Morus Rubra Pollen; Rumex Acetosella Pollen; Populus Alba Pollen.

Product ID43406-0106_50f235f6-940b-49a5-aff2-a2344e8d22ec
NDC43406-0106
Product TypeHuman Otc Drug
Proprietary NameALLERGY NEW ENGLAND MIX
Generic NameBetula Pubescens Bark, Artemisia Vulgaris Pollen, Plantago Lanceolata Pollen, Acer Pseudoplatanus Pollen, Betula Pubescens Bark, Evernia Prunastri Bark, Armaranthus Retroflexus Pollen, Pinus Massoniana Pollen, Tabuliformis Pollen, Ambrosia Artemisifolia Pollen,
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2007-05-29
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameNatural Creations, Inc.
Substance NameBETULA PUBESCENS BARK; ARTEMISIA VULGARIS POLLEN; PLANTAGO LANCEOLATA POLLEN; ACER PSEUDOPLATANUS POLLEN; EVERNIA PRUNASTRI; AMARANTHUS RETROFLEXUS POLLEN; PINUS MASSONIANA POLLEN; PINUS TABULIFORMIS POLLEN; AMBROSIA ARTEMISIIFOLIA POLLEN; JUNIPERUS VIRGINIANA POLLEN; MORUS RUBRA POLLEN; RUMEX ACETOSELLA POLLEN; POPULUS ALBA POLLEN
Active Ingredient Strength6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 43406-0106-1

30 mL in 1 BOTTLE, SPRAY (43406-0106-1)
Marketing Start Date2016-06-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43406-0106-1 [43406010601]

ALLERGY NEW ENGLAND MIX LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-01
Inactivation Date2020-01-31
Reactivation Date2020-04-01

Drug Details

Active Ingredients

IngredientStrength
BETULA PUBESCENS BARK6 [hp_X]/mL

OpenFDA Data

SPL SET ID:b12b20c3-a7bf-4366-89da-a8023204048e
Manufacturer
UNII
UPC Code
  • 0877730003843

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