44911-0911 NDC - CHEMSTAT (GLYCERINUM, TARAXACUM OFFICINALE, PHYTOLACCA DECANDRA, ARSENICUM ALBUM, BOVISTA, CARBO VEGETABILIS, CARBONEUM SULPHURATUM, COFFEA CRUDA, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SULPHUR, ACETYLSALICYLICUM ACIDUM, FORMALINUM, GLONOINUM, INSULINUM (HUMAN), LITHIUM CARBONICUM, TEREBINTHINA, THYROIDINUM (SUIS), ACETICUM ACIDUM, BENZOICUM ACIDUM, BENZYL ALCOHOL, BORICUM ACIDUM, CHLORINUM, CORTISONE ACETICUM, EUGENOL, FOLLICULINUM, ISOPROPYL PALMITATE, LACTICUM ACIDUM,)

Drug Information

  • Product NDC: 44911-0911
  • Proprietary Name: Chemstat
  • Non Proprietary Name: Glycerinum, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Bovista, Carbo Vegetabilis, Carboneum Sulphuratum, Coffea Cruda, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Phosphorus, Sulphur, Acetylsalicylicum Acidum, Formalinum, Glonoinum, Insulinum (Human), Lithium Carbonicum, Terebinthina, Thyroidinum (Suis), Aceticum Acidum, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum,
  • Active Ingredient(s): 12 [hp_X]/mL ACETIC ACID; 12 [hp_X]/mL ACTIVATED CHARCOAL; 12 [hp_X]/mL ARABICA COFFEE BEAN; 12 [hp_X]/mL ARSENIC TRIOXIDE; 12 [hp_X]/mL ASPIRIN; 12 [hp_X]/mL BENZOIC ACID; 12 [hp_X]/mL BENZYL ALCOHOL; 12 [hp_X]/mL BORIC ACID; 12 [hp_X]/mL CARBON DISULFIDE; 12 [hp_X]/mL CHLORINE; 15 [hp_C]/mL CORTICOTROPIN; 12 [hp_X]/mL CORTISONE ACETATE; 12 [hp_X]/mL ESTRONE; 12 [hp_X]/mL EUGENOL; 12 [hp_X]/mL FORMALDEHYDE SOLUTION; 3 [hp_X]/mL GLYCERIN; 12 [hp_X]/mL INSULIN HUMAN; 12 [hp_X]/mL ISOPROPYL PALMITATE; 12 [hp_X]/mL KEROSENE; 12 [hp_X]/mL LACTIC ACID, DL-; 12 [hp_X]/mL LEAD; 12 [hp_X]/mL LITHIUM CARBONATE; 12 [hp_X]/mL LYCOPERDON UTRIFORME FRUITING BODY; 12 [hp_X]/mL NITRIC ACID; 12 [hp_X]/mL NITROGLYCERIN; 12 [hp_X]/mL PETROLATUM; 12 [hp_Q]/mL PHENYLBUTAZONE; 12 [hp_X]/mL PHOSPHORIC ACID; 12 [hp_X]/mL PHOSPHORUS; 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 12 [hp_X]/mL POTASSIUM SORBATE; 12 [hp_X]/mL RESORCINOL; 12 [hp_X]/mL SALICYLIC ACID; 12 [hp_X]/mL SORBITOL; 12 [hp_X]/mL STEARYL ALCOHOL; 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 12 [hp_X]/mL SULFUR; 3 [hp_X]/mL TARAXACUM OFFICINALE; 12 [hp_X]/mL THYROID; 12 [hp_X]/mL TURPENTINE OIL; 12 [hp_X]/mL XYLITOL
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenocorticotropic Hormone [CS]; Adrenocorticotropic Hormone [EPC]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Ammonium Ion Binding Activity [MoA]; Anti-Inflammatory Agents; Non-Steroidal [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Cyclooxygenase Inhibitors [MoA]; Decreased Platelet Aggregation [PE]; Decreased Prostaglandin Production [PE]; Dietary Proteins [CS]; Glycerol [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Insulin [CS]; Insulin [EPC]; Mood Stabilizer [EPC]; Nitrate Vasodilator [EPC]; Nitrates [CS]; Nitrogen Binding Agent [EPC]; Non-Standardized Chemical Allergen [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Nonsteroidal Anti-inflammatory Drug [EPC]; Pediculicide [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Platelet Aggregation Inhibitor [EPC]; Seed Storage Proteins [CS]; Seed Storage Proteins [CS]; Standardized Chemical Allergen [EPC]; Vasodilation [PE]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/25/2026

Package Information

No. Package Code Package Description Billing Unit
144911-0911-130 mL in 1 BOTTLE, DROPPER (44911-0911-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0911The 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 NAMEChemstatThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGlycerinum, Taraxacum Officinale, Phytolacca Decandra, Arsenicum Album, Bovista, Carbo Vegetabilis, Carboneum Sulphuratum, Coffea Cruda, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Phosphorus, Sulphur, Acetylsalicylicum Acidum, Formalinum, Glonoinum, Insulinum (Human), Lithium Carbonicum, Terebinthina, Thyroidinum (Suis), Aceticum Acidum, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum,The 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 DATE6/25/2026This 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 NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETIC ACID; ACTIVATED CHARCOAL; ARABICA COFFEE BEAN; ARSENIC TRIOXIDE; ASPIRIN; BENZOIC ACID; BENZYL ALCOHOL; BORIC ACID; CARBON DISULFIDE; CHLORINE; CORTICOTROPIN; CORTISONE ACETATE; ESTRONE; EUGENOL; FORMALDEHYDE SOLUTION; GLYCERIN; INSULIN HUMAN; ISOPROPYL PALMITATE; KEROSENE; LACTIC ACID, DL-; LEAD; LITHIUM CARBONATE; LYCOPERDON UTRIFORME FRUITING BODY; NITRIC ACID; NITROGLYCERIN; PETROLATUM; PHENYLBUTAZONE; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM SORBATE; RESORCINOL; SALICYLIC ACID; SORBITOL; STEARYL ALCOHOL; STRYCHNOS NUX-VOMICA SEED; SULFUR; TARAXACUM OFFICINALE; THYROID; TURPENTINE OIL; XYLITOLAn 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; 15; 12; 12; 12; 12; 3; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 6; 12; 12; 12; 12; 12; 12; 12; 3; 12; 12; 12 
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_C]/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; [hp_X]/mL; [hp_X]/mL; [hp_Q]/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; [hp_X]/mL 
PHARM CLASSESAdrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Dietary Proteins [CS], Glycerol [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Insulin [CS], Insulin [EPC], Mood Stabilizer [EPC], Nitrate Vasodilator [EPC], Nitrates [CS], Nitrogen Binding Agent [EPC], Non-Standardized Chemical Allergen [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Pediculicide [EPC], Plant Proteins [CS], Plant Proteins [CS], Platelet Aggregation Inhibitor [EPC], Seed Storage Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC], Vasodilation [PE] 

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This page was last updated on: 7/7/2026

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