NDC 60986-1021

CACTUS

Cactus Grandiflorus, Convallaria Majalis, Crataegus Laevigata, Camphora, Kalmia Latifolia, Spigelia Anthelmia, Lachesis Mutus, Arnica Montana,tabacum, Glonoinum

CACTUS is a Oral Liquid in the Human Prescription Drug category. It is labeled and distributed by Marco Pharma International Llc.. The primary component is Selenicereus Grandiflorus Stem; Convallaria Majalis; Crataegus Laevigata Whole; Camphor (natural); Kalmia Latifolia Leaf; Spigelia Anthelmia; Lachesis Muta Venom; Arnica Montana; Tobacco Leaf; Nitroglycerin.

• Product ID: 60986-1021_d9f66e0a-0f79-43af-b59e-b2984e9a8850
• NDC: 60986-1021
• Product Type: Human Prescription Drug
• Proprietary Name: CACTUS
• Generic Name: Cactus Grandiflorus, Convallaria Majalis, Crataegus Laevigata, Camphora, Kalmia Latifolia, Spigelia Anthelmia, Lachesis Mutus, Arnica Montana,tabacum, Glonoinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 1992-03-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Marco Pharma International LLC.
• Substance Name: SELENICEREUS GRANDIFLORUS STEM; CONVALLARIA MAJALIS; CRATAEGUS LAEVIGATA WHOLE; CAMPHOR (NATURAL); KALMIA LATIFOLIA LEAF; SPIGELIA ANTHELMIA; LACHESIS MUTA VENOM; ARNICA MONTANA; TOBACCO LEAF; NITROGLYCERIN
• Active Ingredient Strength: 2 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
• Pharm Classes: Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],Plant Proteins [CS],Nitrate Vasodilator [EPC],Nitrates [CS],Vasodilation [PE]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 60986-1021-3

50 mL in 1 BOTTLE, GLASS (60986-1021-3)

• Marketing Start Date: 1992-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60986-1021-3 [60986102103]

CACTUS LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1992-03-01
• Inactivation Date: 2019-11-13

NDC 60986-1021-4 [60986102104]

CACTUS LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1992-03-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
SELENICEREUS GRANDIFLORUS STEM	2 [hp_X]/100mL

OpenFDA Data

• SPL SET ID: 9504b8f5-2b4f-412b-93b4-d8d542aea6c9
• Manufacturer:
  • Marco Pharma International LLC.
• UNII:
  • WYT05213GE
  • EFX9G567MJ
  • O80TY208ZW
  • QHH4HVF5QE
  • 7114SV0MYK
  • VSW71SS07I
  • 79N6542N18
  • 6YR2608RSU
  • N20HL7Q941
  • G59M7S0WS3

Pharmacological Class

• Non-Standardized Plant Allergenic Extract [EPC]
• Increased Histamine Release [PE]
• Cell-mediated Immunity [PE]
• Increased IgG Production [PE]
• Allergens [CS]
• Plant Proteins [CS]
• Nitrate Vasodilator [EPC]
• Nitrates [CS]
• Vasodilation [PE]

NDC Crossover Matching brand name "CACTUS" or generic name "Cactus Grandiflorus, Convallaria Majalis, Crataegus Laevigata, Camphora, Kalmia Latifolia, Spigelia Anthelmia, Lachesis Mutus, Arnica Montana,tabacum, Glonoinum"

NDC	Brand Name	Generic Name
60986-1021	CACTUS	CACTUS GRANDIFLORUS, CONVALLARIA MAJALIS, CRATAEGUS LAEVIGATA, CAMPHORA, KALMIA LATIFOLIA, SPIGELIA ANTHELMIA, LACHESIS MUTUS, ARNICA MONTANA,TABACUM, GLONOINUM
60986-1028	CACTUS	Crataegus laevigata, Cactus grandiflorus, convallaria majalis, camphor, kalmia latifolia, spigelia anthelmia, Lachesis mutus, Arnica montana, tabacum, glonoinum