Day And Night Vitals

Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir

Net Remedies
Human Prescription Drug
NDC 61626-0100

Day And Night Vitals also known as Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir is a human prescription drug labeled by 'Net Remedies'. National Drug Code (NDC) number for Day And Night Vitals is 61626-0100. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Day And Night Vitals drug includes Aloe Vera Leaf - 12 [hp_X]/59mL Arsenic Trioxide - 12 [hp_X]/59mL Berberis Vulgaris Root Bark - 12 [hp_X]/59mL Ceanothus Americanus Leaf - 12 [hp_X]/59mL Chelidonium Majus - 12 [hp_X]/59mL Cholesterol - 12 [hp_X]/59mL Clematis Recta Flowering Top - 12 [hp_X]/59mL Dibasic Potassium Phosphate - 12 [hp_X]/59mL Gamboge - 12 [hp_X]/59mL Garlic - 12 [hp_X]/59mL and more. The currest status of Day And Night Vitals drug is Active.

Drug Information:

Drug NDC:	61626-0100
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Day And Night Vitals
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Net Remedies
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ALOE VERA LEAF - 12 [hp_X]/59mL ARSENIC TRIOXIDE - 12 [hp_X]/59mL BERBERIS VULGARIS ROOT BARK - 12 [hp_X]/59mL CEANOTHUS AMERICANUS LEAF - 12 [hp_X]/59mL CHELIDONIUM MAJUS - 12 [hp_X]/59mL CHOLESTEROL - 12 [hp_X]/59mL CLEMATIS RECTA FLOWERING TOP - 12 [hp_X]/59mL DIBASIC POTASSIUM PHOSPHATE - 12 [hp_X]/59mL GAMBOGE - 12 [hp_X]/59mL GARLIC - 12 [hp_X]/59mL Load more... HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 12 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/59mL MARSDENIA CONDURANGO BARK - 12 [hp_X]/59mL PASSIFLORA INCARNATA TOP - 12 [hp_X]/59mL POTASSIUM BROMIDE - 12 [hp_X]/59mL SENNA LEAF - 12 [hp_X]/59mL SILICON DIOXIDE - 12 [hp_X]/59mL SODIUM CARBONATE - 12 [hp_X]/59mL SOLIDAGO VIRGAUREA FLOWERING TOP - 12 [hp_X]/59mL SPIGELIA ANTHELMIA - 12 [hp_X]/59mL SPONGIA OFFICINALIS SKELETON, ROASTED - 12 [hp_X]/59mL TRIBASIC CALCIUM PHOSPHATE - 12 [hp_X]/59mL VERATRUM VIRIDE ROOT - 12 [hp_X]/59mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	04 Dec, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	29 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	NET Remedies
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0016962
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	ZY81Z83H0X S7V92P67HO 1TH8Q20J0U 25B1Y14T8N 7E889U5RNN 97C5T2UQ7J 396421SP9F CI71S98N1Z 7556HJ7587 V1V998DC17 Load more... T7S323PKJS C88X29Y479 R23QIR6YBA CLF5YFS11O OSD78555ZM AK7JF626KX ETJ7Z6XBU4 45P3261C7T 5405K23S50 WYT05213GE 1PIP394IID 91D9GV0Z28 197B3Q7T5Q
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Coagulation Factor Activity [PE] Increased Histamine Release [PE] Non-Standardized Food Allergenic Extract [EPC] Plant Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
61626-0100-4	59 mL in 1 BOTTLE (61626-0100-4)	04 Dec, 2018	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Day And Night Vitals

Allium Sat & more..

Liquid
NET Remedies
NDC: 61626-0100

Purpose:

Indications for use: for the temporary relief of symptoms related to low vitality and function of the large intestine, stomach, spleen, heart, small intestine, bladder, kidney, sex organs, thyroid, adrenal, gall bladder, liver and lung.**

Product Elements:

Day and night vitals allium sat, aloe, arsenicum alb, berber vulg, calc phos, ceanothus, chelidonium maj, cholesterinum, clematis erecta, condurango, gambogia, hamamelis, kali brom, kali phos, lycopodium, nat carb, passiflora, senna, silicea, solidago, spigelia anth, spongia, veratrum vir citric acid monohydrate potassium sorbate water garlic garlic aloe vera leaf aloe vera leaf arsenic trioxide arsenic cation (3+) berberis vulgaris root bark berberis vulgaris root bark tribasic calcium phosphate calcium cation ceanothus americanus leaf ceanothus americanus leaf chelidonium majus chelidonium majus cholesterol cholesterol clematis recta flowering top clematis recta flowering top marsdenia condurango bark marsdenia condurango bark gamboge gamboge hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark potassium bromide bromide ion dibasic potassium phosphate phosphate ion lycopodium clavatum spore lycopodium clavatum spore sodium carbonate carbonate ion passiflora incarnata top passiflora incarnata flowering top senna leaf senna leaf silicon dioxide silicon dioxide solidago virgaurea flowering top solidago virgaurea flowering top spigelia anthelmia spigelia anthelmia spongia officinalis skeleton, roasted spongia officinalis skeleton, roasted veratrum viride root veratrum viride root

Indications and Usage:

âindications for use: âfor the temporary relief of symptoms related to low vitality and function of the large intestine, stomach, spleen, heart, small intestine, bladder, kidney, sex organs, thyroid, adrenal, gall bladder, liver and lung.**

Warnings:

âwarnings: ââ¢ âif symptoms persist or worsen â, seek advice of licensed health care practitioner. â¢ âif pregnant or nursing, âtake only on advice of licensed health care practitioner. â¢ âkeep this and all medication out of reach of children. â¢ keep this and all medication out of reach of children.

Dosage and Administration:

âdirections: âspray 9-12 pumps (approximately 1/2 tsp.) directly in mouth 3 times a day or as directed by a licensed health care practitioner. when appropriate, also spray externally on complaint area 3 times daily.

Package Label Principal Display Panel:

Net remedies #24 homeopathic preparation 24-hour support âprofessional formula â ânaturally no side effects â â â â 2 fl oz (59 ml) day and night vitals 2 oz bottle label indications for use: for the temporary relief of symptoms related to low vitality and function of the large intestine, stomach, spleen, heart, small intestine, bladder, kidney, sex organs, thyroid, adrenal, gall bladder, liver and lung.**

Further Questions:

âwww.netmindbody.com made in the usa.

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.