83027-0054 NDC - SKIN LIQUESCENCE (ANGELICA ARCHANGELICA, BERBERIS AQUIFOLIUM, BERBERIS VULGARIS, EQUISETUM ARVENSE, GERANIUM MACULATUM, MYRRHA, IRIS VERSICOLOR, THUJA OCCIDENTALIS, NUX VOMICA, HYPERICUM PERFORATUM, HUMAN GROWTH HORMONE (HGH), MERCURIUS SOLUBILIS, PETROLEUM, GRAPHITES)

Drug Information

  • Product NDC: 83027-0054
  • Proprietary Name: Skin Liquescence
  • Non Proprietary Name: Angelica Archangelica, Berberis Aquifolium, Berberis Vulgaris, Equisetum Arvense, Geranium Maculatum, Myrrha, Iris Versicolor, Thuja Occidentalis, Nux Vomica, Hypericum Perforatum, Human Growth Hormone (HGH), Mercurius Solubilis, Petroleum, Graphites
  • Active Ingredient(s): 3 [hp_X]/mL ANGELICA ARCHANGELICA ROOT; 3 [hp_X]/mL BERBERIS AQUIFOLIUM ROOT BARK; 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 3 [hp_X]/mL EQUISETUM ARVENSE TOP; 3 [hp_X]/mL GERANIUM MACULATUM ROOT; 16 [hp_X]/mL GRAPHITE; 10 [hp_X]/mL HYPERICUM PERFORATUM WHOLE; 4 [hp_X]/mL IRIS VERSICOLOR ROOT; 12 [hp_X]/mL KEROSENE; 12 [hp_X]/mL MERCURIUS SOLUBILIS; 3 [hp_X]/mL MYRRH; 12 [hp_X]/mL SOMATROPIN; 8 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 6 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Human Growth Hormone [CS]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Recombinant Human Growth Hormone [EPC]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Nutritional Specialties, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/17/2023

Package Information

No. Package Code Package Description Billing Unit
183027-0054-1120 mL in 1 BOTTLE, GLASS (83027-0054-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83027-0054The 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 OTC 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 NAMESkin LiquescenceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAngelica Archangelica, Berberis Aquifolium, Berberis Vulgaris, Equisetum Arvense, Geranium Maculatum, Myrrha, Iris Versicolor, Thuja Occidentalis, Nux Vomica, Hypericum Perforatum, Human Growth Hormone (HGH), Mercurius Solubilis, Petroleum, GraphitesThe 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 DATE4/17/2023This 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 NAMENutritional Specialties, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANGELICA ARCHANGELICA ROOT; BERBERIS AQUIFOLIUM ROOT BARK; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; GERANIUM MACULATUM ROOT; GRAPHITE; HYPERICUM PERFORATUM WHOLE; IRIS VERSICOLOR ROOT; KEROSENE; MERCURIUS SOLUBILIS; MYRRH; SOMATROPIN; STRYCHNOS NUX-VOMICA SEED; THUJA OCCIDENTALIS LEAFY TWIGAn 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 STRENGTH3; 3; 3; 3; 3; 16; 10; 4; 12; 12; 3; 12; 8; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Human Growth Hormone [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Recombinant Human Growth Hormone [EPC], Seed Storage Proteins [CS] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 11/21/2025

Previous Code
Next Code