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Cutis Compositum - 50114-7050-1 - (LEDUM PALUSTRE TWIG and URTICA URENS and AESCULUS HIPPOCASTANUM FLOWER and GALIUM APARINE and STRYCHNOS IGNATII SEED and ARCTIUM LAPPA ROOT and PHOSPHORIC ACID and SUS SCROFA SKIN and THUJA OCCIDENTALIS LEAFY TWIG and FUMARIC ACID and SUS SCROFA UMBILICAL CORD and SUS SCROFA ADRENAL GLAND and PORK LIVER and .ALPHA.-KETOGLUTARIC ACID and SODIUM DIETHYL OXALACETATE and SUS SCROFA PLACENTA and SELENIUM and SUS SCROFA SPLEEN)

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Drug Information of Cutis Compositum

Product NDC: 50114-7050
Proprietary Name: Cutis Compositum
Non Proprietary Name: LEDUM PALUSTRE TWIG and URTICA URENS and AESCULUS HIPPOCASTANUM FLOWER and GALIUM APARINE and STRYCHNOS IGNATII SEED and ARCTIUM LAPPA ROOT and PHOSPHORIC ACID and SUS SCROFA SKIN and THUJA OCCIDENTALIS LEAFY TWIG and FUMARIC ACID and SUS SCROFA UMBILICAL CORD and SUS SCROFA ADRENAL GLAND and PORK LIVER and .ALPHA.-KETOGLUTARIC ACID and SODIUM DIETHYL OXALACETATE and SUS SCROFA PLACENTA and SELENIUM and SUS SCROFA SPLEEN
Active Ingredient(s): 10; 6; 6; 13; 28; 198; 10; 6; 28; 4; 13; 6; 10; 10; 10; 6; 10; 10; 10; 8; 10; 10; 13; 8; 4    [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL & nbsp;   LEDUM PALUSTRE TWIG and URTICA URENS and AESCULUS HIPPOCASTANUM FLOWER and GALIUM APARINE and STRYCHNOS IGNATII SEED and ARCTIUM LAPPA ROOT and PHOSPHORIC ACID and SUS SCROFA SKIN and THUJA OCCIDENTALIS LEAFY TWIG and FUMARIC ACID and SUS SCROFA UMBILICAL CORD and SUS SCROFA ADRENAL GLAND and PORK LIVER and .ALPHA.-KETOGLUTARIC ACID and SODIUM DIETHYL OXALACETATE and SUS SCROFA PLACENTA and SELENIUM and SUS SCROFA SPLEEN
Administration Route(s): INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cutis Compositum

Product NDC: 50114-7050
Labeler Name: Heel Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20090430

Package Information of Cutis Compositum

Package NDC: 50114-7050-1
Package Description: 10 VIAL in 1 CARTON (50114-7050-1) > 2.2 mL in 1 VIAL

NDC Information of Cutis Compositum

NDC Code 50114-7050-1
Proprietary Name Cutis Compositum
Package Description 10 VIAL in 1 CARTON (50114-7050-1) > 2.2 mL in 1 VIAL
Product NDC 50114-7050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEDUM PALUSTRE TWIG and URTICA URENS and AESCULUS HIPPOCASTANUM FLOWER and GALIUM APARINE and STRYCHNOS IGNATII SEED and ARCTIUM LAPPA ROOT and PHOSPHORIC ACID and SUS SCROFA SKIN and THUJA OCCIDENTALIS LEAFY TWIG and FUMARIC ACID and SUS SCROFA UMBILICAL CORD and SUS SCROFA ADRENAL GLAND and PORK LIVER and .ALPHA.-KETOGLUTARIC ACID and SODIUM DIETHYL OXALACETATE and SUS SCROFA PLACENTA and SELENIUM and SUS SCROFA SPLEEN
Dosage Form Name INJECTION
Route Name INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20090430
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name .ALPHA.-KETOGLUTARIC ACID; AESCULUS HIPPOCASTANUM FLOWER; ARCTIUM LAPPA ROOT; CALCIUM FLUORIDE; CORTISONE ACETATE; FORMIC ACID; FUMARIC ACID; GALIUM APARINE; ICHTHAMMOL; LEDUM PALUSTRE TWIG; MERCURIUS SOLUBILIS; PHOSPHORIC ACID; PORK LIVER; SELENIUM; SODIUM DIETHYL OXALACETATE; STRYCHNOS IGNATII SEED; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA PLACENTA; SUS SCROFA SKIN; SUS SCROFA SPLEEN; SUS SCROFA UMBILICAL CORD; THALLIUM SULFATE; THUJA OCCIDENTALIS LEAFY TWIG; URTICA URENS
Strength Number 10; 6; 6; 13; 28; 198; 10; 6; 28; 4; 13; 6; 10; 10; 10; 6; 10; 10; 10; 8; 10; 10; 13; 8; 4
Strength Unit [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL
Pharmaceutical Classes Non-Standardized Animal Skin Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Cells, Epidermal [Chemical/Ingredient],Allergens [Chemical/Ingredient]

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