61626-0100 NDC - 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)

Drug Information

  • Product NDC: 61626-0100
  • Proprietary Name: Day and Night Vitals
  • 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
  • Active Ingredient(s): 12 [hp_X]/59mL 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 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
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): 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]

Labeler Information

Field Name Field Value
Labeler Name: NET Remedies
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/4/2018

Package Information

No. Package Code Package Description Billing Unit
161626-0100-459 mL in 1 BOTTLE (61626-0100-4)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61626-0100The 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.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMEDay and Night VitalsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAllium 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 virThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/4/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMENET RemediesName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALOE VERA LEAF; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; CHOLESTEROL; CLEMATIS RECTA FLOWERING TOP; DIBASIC POTASSIUM PHOSPHATE; GAMBOGE; GARLIC; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; LYCOPODIUM CLAVATUM SPORE; MARSDENIA CONDURANGO BARK; PASSIFLORA INCARNATA TOP; POTASSIUM BROMIDE; SENNA LEAF; SILICON DIOXIDE; SODIUM CARBONATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SPIGELIA ANTHELMIA; SPONGIA OFFICINALIS SKELETON, ROASTED; TRIBASIC CALCIUM PHOSPHATE; VERATRUM VIRIDE ROOTAn 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.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAllergens [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] 

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This page was last updated on: 12/6/2025

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