NDC 55714-4402 Eczema Skin Care
Antimon. Crud., Arsenicum Alb., Berber. Vulg., Bovista , Bryonia , Cantharis , Chelidonium Majus, Croton, Dulcamara, Graphites, Hepar Sulph. Calc., Lycopodium Mezereum, Nux Vom, Petroleum, Pulex Irritans, Pulsatilla, Rhus Toxicodendron, Sarsaparilla, Sepia, Sulphur Iod, Echinacea, Rumex Crisp., Taraxacum , Urtica Ur., Echinacea, Rumex Crisp., Taraxacum, Urtica Ur.
NDC Product Code 55714-4402
Proprietary Name: Eczema Skin Care 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: Antimon. Crud., Arsenicum Alb., Berber. Vulg., Bovista , Bryonia , Cantharis , Chelidonium Majus, Croton, Dulcamara, Graphites, Hepar Sulph. Calc., Lycopodium Mezereum, Nux Vom, Petroleum, Pulex Irritans, Pulsatilla, Rhus Toxicodendron, Sarsaparilla, Sepia, Sulphur Iod, Echinacea, Rumex Crisp., Taraxacum , Urtica Ur., Echinacea, Rumex Crisp., Taraxacum, Urtica Ur. 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.
Code Structure
- 55714 - Newton Laboratories, Inc.
- 55714-4402 - Eczema Skin Care
NDC 55714-4402-1
Package Description: 29.57 mL in 1 BOTTLE, GLASS
NDC 55714-4402-2
Package Description: 59.14 mL in 1 BOTTLE, GLASS
NDC Product Information
Eczema Skin Care with NDC 55714-4402 is a a human prescription drug product labeled by Newton Laboratories, Inc.. The generic name of Eczema Skin Care is antimon. crud., arsenicum alb., berber. vulg., bovista , bryonia , cantharis , chelidonium majus, croton, dulcamara, graphites, hepar sulph. calc., lycopodium mezereum, nux vom, petroleum, pulex irritans, pulsatilla, rhus toxicodendron, sarsaparilla, sepia, sulphur iod, echinacea, rumex crisp., taraxacum , urtica ur., echinacea, rumex crisp., taraxacum, urtica ur.. 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 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.
Eczema Skin Care 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.
- ANTIMONY TRISULFIDE 20 [hp_X]/mL
- ARSENIC TRIOXIDE 20 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 20 [hp_X]/mL
- GIANT PUFFBALL 20 [hp_X]/mL
- BRYONIA ALBA ROOT 20 [hp_X]/mL
- LYTTA VESICATORIA 20 [hp_X]/mL
- CHELIDONIUM MAJUS 20 [hp_X]/mL
- CROTON TIGLIUM SEED 20 [hp_X]/mL
- SOLANUM DULCAMARA TOP 20 [hp_X]/mL
- GRAPHITE 20 [hp_X]/mL
- CALCIUM SULFIDE 20 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 20 [hp_X]/mL
- DAPHNE MEZEREUM BARK 20 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 20 [hp_X]/mL
- KEROSENE 20 [hp_X]/mL
- PULEX IRRITANS 20 [hp_X]/mL
- PULSATILLA VULGARIS 20 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 20 [hp_X]/mL
- SMILAX REGELII ROOT 20 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 20 [hp_X]/mL
- SULFUR IODIDE 20 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 8 [hp_X]/mL
- RUMEX CRISPUS ROOT 8 [hp_X]/mL
- TARAXACUM OFFICINALE 8 [hp_X]/mL
- URTICA URENS 8 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
- RUMEX CRISPUS ROOT 3 [hp_X]/mL
- TARAXACUM OFFICINALE 3 [hp_X]/mL
- URTICA URENS 3 [hp_X]/mL
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.
Pharmacological Class(es)
What is a Pharmacological Class?These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
- Calcium - [CS]
- Calcium - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Allergens - [CS]
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
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: 06-01-2011 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: 12-31-2018 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: E 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.
Eczema Skin Care Product Label Images
Eczema Skin Care 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
- Product Name & Indications Section
- Direction Section
- Active Ingredient Section
- Inactive Ingredient Section
- Questions? Section
- Warnings Section
- Otc - Pregnancy Or Breast Feeding Section
- Otc - Keep Out Of Reach Of Children Section
Product Name & Indications Section
ECZEMA~SKIN CARE Formulated for symptoms associated with seborrhea, eczema, psoriasis, cellulitis, dermatitis, lichen planus and other skin-related conditions.
Direction Section
Directions: ORAL USE ONLY - SHAKE WELL. Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) as needed or as directed by a healthcare professional.
Active Ingredient Section
Antimon. crud. 20x, Arsenicum alb. 20x, Berber. vulg. 20x, Bovista 20x, Bryonia 20x, Cantharis 20x, Chelidonium majus 20x, Croton 20x, Dulcamara 20x, Graphites 20x, Hepar sulph. calc. 20x, Lycopodium 20x, Mezereum 20x, Nux vom. 20x, Petroleum 20x, Pulex irritans 20x, Pulsatilla 20x, Rhus toxicodendron 20x, Sarsaparilla 20x, Sepia 20x, Sulphur iod. 20x, Echinacea 8x, Rumex crisp. 8x, Taraxacum 8x, Urtica ur. 8x, Echinacea 3x, Rumex crisp. 3x, Taraxacum 3x, Urtica ur. 3x.
Inactive Ingredient Section
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.
Questions? Section
Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 -Conyers, GA 30012Questions? 1.800.448.7256
Warnings Section
Warning: Do not use if tamper- evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.
Otc - Pregnancy Or Breast Feeding Section
Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.
Otc - Keep Out Of Reach Of Children Section
Keep out of reach of children.
* Please review the disclaimer below.