Anti Stress Formula Spray
NDC 83027-0085
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Anti Stress Formula (apis mellifica, citrus vulgaris, clematis vitalba, flos, glandula suprarenalis (bovine), helianthemum nummularium, flos, impatiens glandulifera, flos, kali phosphoricum, ornithogalum umbellatum, flos, prunus cerasifera, flos, scutellaria lateriflora, viburnum opulus, cortisone aceticum, aconitum napellus, adrenalinum, dopamine (hydrochloride)) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nutritional Specialties, Inc.. 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 83027-0085 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
83027-0085
Proprietary Name:
Anti Stress Formula
Non-Proprietary Name: [1]
Apis Mellifica, Citrus Vulgaris, Clematis Vitalba, Flos, Glandula Suprarenalis (bovine), Helianthemum Nummularium, Flos, Impatiens Glandulifera, Flos, Kali Phosphoricum, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Scutellaria Lateriflora, Viburnum Opulus, Cortisone Aceticum, Aconitum Napellus, Adrenalinum, Dopamine (hydrochloride)
Substance Name: [2]
Aconitum Napellus Whole; Apis Mellifera; Bos Taurus Adrenal Gland; Citrus Aurantium Fruit Rind; Clematis Vitalba Flower; Cortisone Acetate; Dibasic Potassium Phosphate; Dopamine Hydrochloride; Epinephrine; Helianthemum Nummularium Flower; Impatiens Glandulifera Flower; Ornithogalum Umbellatum Flowering Top; Prunus Cerasifera Flower; Scutellaria Lateriflora Whole; Viburnum Opulus Bark
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:
83027
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]
07-25-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 83027-0085?
The NDC code 83027-0085 is assigned by the FDA to the product Anti Stress Formula. It is commonly known by its generic name, apis mellifica, citrus vulgaris, clematis vitalba, flos, glandula suprarenalis (bovine), helianthemum nummularium, flos, impatiens glandulifera, flos, kali phosphoricum, ornithogalum umbellatum, flos, prunus cerasifera, flos, scutellaria lateriflora, viburnum opulus, cortisone aceticum, aconitum napellus, adrenalinum, dopamine (hydrochloride). This pharmaceutical product is labeled by Nutritional Specialties, Inc. 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: 83027-0085-1. 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?
Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
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.
- ACONITUM NAPELLUS WHOLE 12 [hp_X]/mL
- APIS MELLIFERA 6 [hp_X]/mL
- BOS TAURUS ADRENAL GLAND 6 [hp_X]/mL
- CITRUS AURANTIUM FRUIT RIND 6 [hp_X]/mL
- CLEMATIS VITALBA FLOWER 6 [hp_X]/mL
- CORTISONE ACETATE 6 [hp_X]/mL - 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)
- DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL
- DOPAMINE HYDROCHLORIDE 16 [hp_X]/mL - One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action.
- EPINEPHRINE 12 [hp_X]/mL - 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.
- HELIANTHEMUM NUMMULARIUM FLOWER 6 [hp_X]/mL
- IMPATIENS GLANDULIFERA FLOWER 6 [hp_X]/mL
- ORNITHOGALUM UMBELLATUM FLOWERING TOP 6 [hp_X]/mL
- PRUNUS CERASIFERA FLOWER 6 [hp_X]/mL
- SCUTELLARIA LATERIFLORA WHOLE 6 [hp_X]/mL
- VIBURNUM OPULUS BARK 6 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7) (Active Moiety)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
- DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC) (Active Moiety)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805)
- VIBURNUM OPULUS BARK (UNII: T1UG6H6805) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- DOPAMINE HYDROCHLORIDE (UNII: 7L3E358N9L)
- DOPAMINE (UNII: VTD58H1Z2X) (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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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)
- Allergens - [CS]
- Bee Venoms - [CS]
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
- Corticosteroid - [EPC] (Established Pharmacologic Class)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Standardized Insect Venom Allergenic Extract - [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".
