75053-0008 NDC - APNETEM (PHOSPHORICUM ACIDUM, ALUMEN, PHOSPHORUS, SENEGA OFFICINALIS, ADENOSINUM CYCLOPHOSPHORICUM, ANTIMONIUM TARTARICUM, GRINDELIA, SABADILLA, ALUMINA, CUPRUM METALLICUM, SANGUINARINUM NITRICUM, SILICEA, LACHESIS MUTUS, RHEUM (PALMATUM), ZINCUM METALLICUM, LYCOPODIUM CLAVATUM, MANGANUM PHOSPHORICUM, ANTIPYRINUM, COENZYME A)

Drug Information

  • Product NDC: 75053-0008
  • Proprietary Name: Apnetem
  • Non Proprietary Name: Phosphoricum Acidum, Alumen, Phosphorus, Senega Officinalis, Adenosinum Cyclophosphoricum, Antimonium Tartaricum, Grindelia, Sabadilla, Alumina, Cuprum Metallicum, Sanguinarinum Nitricum, Silicea, Lachesis Mutus, Rheum (Palmatum), Zincum Metallicum, Lycopodium Clavatum, Manganum Phosphoricum, Antipyrinum, Coenzyme A
  • Active Ingredient(s): 9 [hp_X]/mL ADENOSINE CYCLIC PHOSPHATE; 12 [hp_X]/mL ALUMINUM OXIDE; 9 [hp_X]/mL ANTIMONY POTASSIUM TARTRATE; 18 [hp_X]/mL ANTIPYRINE; 12 [hp_C]/mL COENZYME A; 12 [hp_X]/mL COPPER; 9 [hp_X]/mL GRINDELIA HIRSUTULA FLOWERING TOP; 12 [hp_X]/mL LACHESIS MUTA VENOM; 13 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 15 [hp_X]/mL MANGANESE PHOSPHATE, DIBASIC; 6 [hp_X]/mL PHOSPHORIC ACID; 9 [hp_X]/mL PHOSPHORUS; 9 [hp_X]/mL POLYGALA SENEGA ROOT; 6 [hp_X]/mL POTASSIUM ALUM; 12 [hp_X]/mL RHEUM PALMATUM ROOT; 12 [hp_X]/mL SANGUINARINE NITRATE; 9 [hp_X]/mL SCHOENOCAULON OFFICINALE SEED; 12 [hp_X]/mL SILICON DIOXIDE; 12 [hp_X]/mL ZINC
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Inhibit Ovum Fertilization [PE]; Magnetic Resonance Contrast Activity [MoA]; Paramagnetic Contrast Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Nucleic Products, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/18/2021

Package Information

No. Package Code Package Description Billing Unit
175053-0008-1118 mL in 1 BOTTLE, DROPPER (75053-0008-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75053-0008The 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 NAMEApnetemThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPhosphoricum Acidum, Alumen, Phosphorus, Senega Officinalis, Adenosinum Cyclophosphoricum, Antimonium Tartaricum, Grindelia, Sabadilla, Alumina, Cuprum Metallicum, Sanguinarinum Nitricum, Silicea, Lachesis Mutus, Rheum (Palmatum), Zincum Metallicum, Lycopodium Clavatum, Manganum Phosphoricum, Antipyrinum, Coenzyme AThe 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 DATE5/18/2021This 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 NAMENucleic Products, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE CYCLIC PHOSPHATE; ALUMINUM OXIDE; ANTIMONY POTASSIUM TARTRATE; ANTIPYRINE; COENZYME A; COPPER; GRINDELIA HIRSUTULA FLOWERING TOP; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MANGANESE PHOSPHATE, DIBASIC; PHOSPHORIC ACID; PHOSPHORUS; POLYGALA SENEGA ROOT; POTASSIUM ALUM; RHEUM PALMATUM ROOT; SANGUINARINE NITRATE; SCHOENOCAULON OFFICINALE SEED; SILICON DIOXIDE; ZINCAn 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 STRENGTH9; 12; 9; 18; 12; 12; 9; 12; 13; 15; 6; 9; 9; 6; 12; 12; 9; 12; 12 
ACTIVE INGRED UNIT[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 
PHARM CLASSESCopper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC] 

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

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