Appetitego Spray
NDC 68703-351
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Appetitego (adrenalinum, agrimonia eupatoria flos, anacardium, antimon crud, calc carb, castanea sativa flos, cortisone aceticum, fucus, hypothalmus, kali bic, oleander, pituitarum posterium, sabadilla, staphysagria, thyroidinum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Silver Star Brands. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a spray for oral administration. This product entry covers the primary NDC 68703-351 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
68703-351
Proprietary Name:
Appetitego
Non-Proprietary Name: [1]
Adrenalinum, Agrimonia Eupatoria Flos, Anacardium, Antimon Crud, Calc Carb, Castanea Sativa Flos, Cortisone Aceticum, Fucus, Hypothalmus, Kali Bic, Oleander, Pituitarum Posterium, Sabadilla, Staphysagria, Thyroidinum
Substance Name: [2]
Agrimonia Eupatoria Flower; Anacardium Occidentale Fruit; Antimony Trisulfide; Castanea Sativa Flower; Cortisone Acetate; Delphinium Staphisagria Seed; Epinephrine; Fucus Vesiculosus; Nerium Oleander Leaf; Oyster Shell Calcium Carbonate, Crude; Potassium Dichromate; Schoenocaulon Officinale Seed; Sus Scrofa Hypothalamus; Sus Scrofa Pituitary Gland, Posterior; Thyroid, Unspecified
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Spray
- A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
68703
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
08-10-2013
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 68703-351?
The NDC code 68703-351 is assigned by the FDA to the product Appetitego. It is commonly known by its generic name, adrenalinum, agrimonia eupatoria flos, anacardium, antimon crud, calc carb, castanea sativa flos, cortisone aceticum, fucus, hypothalmus, kali bic, oleander, pituitarum posterium, sabadilla, staphysagria, thyroidinum. This pharmaceutical product is labeled by Silver Star Brands and is currently categorized as listed product. The medication is a spray administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 68703-351-59. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 tiems daily. use additionally as needed. Adults: 3 pump sprays. Children 2-12 : 2 pump sprays.
What are Active Ingredients of this product?
An 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.
- AGRIMONIA EUPATORIA FLOWER 10 [hp_X]/59mL
- ANACARDIUM OCCIDENTALE FRUIT 10 [hp_X]/59mL
- ANTIMONY TRISULFIDE 10 [hp_X]/59mL - structure given in first source
- CASTANEA SATIVA FLOWER 10 [hp_X]/59mL
- CORTISONE ACETATE 10 [hp_X]/59mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
- DELPHINIUM STAPHISAGRIA SEED 10 [hp_X]/59mL
- EPINEPHRINE 10 [hp_X]/59mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
- FUCUS VESICULOSUS 10 [hp_X]/59mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
- NERIUM OLEANDER LEAF 10 [hp_X]/59mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 10 [hp_X]/59mL
- POTASSIUM DICHROMATE 10 [hp_X]/59mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
- SCHOENOCAULON OFFICINALE SEED 10 [hp_X]/59mL
- SUS SCROFA HYPOTHALAMUS 10 [hp_X]/59mL
- SUS SCROFA PITUITARY GLAND, POSTERIOR 10 [hp_X]/59mL
- THYROID, UNSPECIFIED 10 [hp_X]/59mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND, POSTERIOR (UNII: E8S87O660T) (Active Moiety)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
- SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E)
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (Active Moiety)
- CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
- CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
Which are the Inactive Ingredients associated UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
- Corticosteroid - [EPC] (Established Pharmacologic Class)
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
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Product & Regulatory Definitions
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.
What is the Substance Name? An 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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
