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GUNA-ALLERGY T - 17089-418-18 - (AMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OP)

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Drug Information of GUNA-ALLERGY T

Product NDC: 17089-418
Proprietary Name: GUNA-ALLERGY T
Non Proprietary Name: AMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OP
Active Ingredient(s): 30; 200; 30; 12; 30; 30; 6; 12; 200; 12; 4; 30; 30; 30; 12; 200; 200    [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL & nbsp;   AMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OP
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-ALLERGY T

Product NDC: 17089-418
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100527

Package Information of GUNA-ALLERGY T

Package NDC: 17089-418-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-418-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-ALLERGY T

NDC Code 17089-418-18
Proprietary Name GUNA-ALLERGY T
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-418-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-418
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AMMONIUM CARBONATE - APIS MELLIFERA - ARSENIC TRIOXIDE - BLATTA ORIENTALIS - CUPRIC ACETATE - DRIMIA MARITIMA BULB - EPINEPHRINE - GALPHIMIA GLAUCA FLOWERING TOP - HISTAMINE DIHYDROCHLORIDE - LUFFA OP
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20100527
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name AMMONIUM CARBONATE; APIS MELLIFERA; ARSENIC TRIOXIDE; BLATTA ORIENTALIS; CUPRIC ACETATE; DRIMIA MARITIMA BULB; EPINEPHRINE; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; MANGANESE GLUCONATE; ONION; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA BRONCHUS; SUS SCROFA NASAL MUCOSA
Strength Number 30; 200; 30; 12; 30; 30; 6; 12; 200; 12; 4; 30; 30; 30; 12; 200; 200
Strength Unit [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
Pharmaceutical Classes

Complete Information of GUNA-ALLERGY T


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