NDC 55714-2310 Dust - Mold - Dander

Dust - Mold - Dander with NDC 55714-2310 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Dust - Mold - Dander is felis catus skin, canis lupus familiaris skin, ortcyolagus cuniculus skin, equus caballus skin, serinus canaria feather, gallus gallus feather, anas platyrhynchos feather, anser anser feather, melopsittacus undulatus feather, phasianus colchicus feather, meleagris gallopavo feather, felis catus hair, human dander, canis lupus familiaris hair, equus caballus hair, oryctolagus cuniculus hair, human hair, human skin, sheep wool, bos taurus hair, capra hircus hair, cavia porcellus hair. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

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 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.

Dust - Mold - Dander 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.

• FELIS CATUS SKIN 60 [hp_X]/mL
• CANIS LUPUS FAMILIARIS SKIN 60 [hp_X]/mL
• ORYCTOLAGUS CUNICULUS SKIN 60 [hp_X]/mL
• EQUUS CABALLUS SKIN 60 [hp_X]/mL
• SERINUS CANARIA FEATHER 60 [hp_X]/mL
• GALLUS GALLUS FEATHER 60 [hp_X]/mL
• ANAS PLATYRHYNCHOS FEATHER 60 [hp_X]/mL
• ANSER ANSER FEATHER 60 [hp_X]/mL
• MELOPSITTACUS UNDULATUS FEATHER 60 [hp_X]/mL
• PHASIANUS COLCHICUS FEATHER 60 [hp_X]/mL
• MELEAGRIS GALLOPAVO FEATHER 60 [hp_X]/mL
• FELIS CATUS HAIR 60 [hp_X]/mL
• HUMAN DANDER 60 [hp_X]/mL
• CANIS LUPUS FAMILIARIS HAIR 60 [hp_X]/mL
• EQUUS CABALLUS HAIR 60 [hp_X]/mL
• ORYCTOLAGUS CUNICULUS HAIR 60 [hp_X]/mL
• HUMAN HAIR 60 [hp_X]/mL
• HUMAN SKIN 60 [hp_X]/mL
• SHEEP WOOL 60 [hp_X]/mL
• BOS TAURUS HAIR 60 [hp_X]/mL
• CAPRA HIRCUS HAIR 60 [hp_X]/mL
• CAVIA PORCELLUS HAIR 60 [hp_X]/mL
• MESOCRICETUS AURATUS HAIR 60 [hp_X]/mL
• WHEAT GLUTEN 15 [hp_X]/mL
• ASPERGILLUS NIGER VAR. NIGER 15 [hp_X]/mL
• CLADOSPORIUM HERBARUM 15 [hp_X]/mL
• HOUSE DUST 15 [hp_X]/mL
• CANDIDA ALBICANS 15 [hp_X]/mL
• HISTAMINE DIHYDROCHLORIDE 15 [hp_X]/mL
• SACCHAROMYCES CEREVISIAE 15 [hp_X]/mL
• USTILAGO MAYDIS 15 [hp_X]/mL
• ANTIMONY TRISULFIDE 10 [hp_X]/mL
• APIS MELLIFERA 10 [hp_X]/mL
• ARSENIC TRIOXIDE 10 [hp_X]/mL
• BAPTISIA TINCTORIA ROOT 10 [hp_X]/mL
• BLATTA ORIENTALIS 10 [hp_X]/mL
• BROMINE 10 [hp_X]/mL
• BRYONIA ALBA ROOT 10 [hp_X]/mL
• CENTAUREA BENEDICTA 10 [hp_X]/mL
• CHELIDONIUM MAJUS 10 [hp_X]/mL
• CINCHONA OFFICINALIS BARK 10 [hp_X]/mL
• IPECAC 10 [hp_X]/mL
• LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/mL
• STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/mL
• PODOPHYLLUM 10 [hp_X]/mL
• TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL
• SILICON DIOXIDE 10 [hp_X]/mL
• IRIS VERSICOLOR ROOT 3 [hp_X]/mL
• SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/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.

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

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: Newton Laboratories, Inc.
Labeler Code: 55714
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: 03-01-2011 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: 12-31-2019 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’.

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