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GUNA-ARTHRO - 17089-304-18 - (.ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -)

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Drug Information of GUNA-ARTHRO

Product NDC: 17089-304
Proprietary Name: GUNA-ARTHRO
Non Proprietary Name: .ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -
Active Ingredient(s): 3; 3; 3; 3; 6; 6; 6; 6; 6; 3; 4; 6; 3; 3; 6; 6; 3; 6; 6; 6; 6; 6; 6; 6; 6; 6; 4    [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_C]/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_C]/30mL & nbsp;   .ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-ARTHRO

Product NDC: 17089-304
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060523

Package Information of GUNA-ARTHRO

Package NDC: 17089-304-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-304-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-ARTHRO

NDC Code 17089-304-18
Proprietary Name GUNA-ARTHRO
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-304-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-304
Product Type Name HUMAN OTC DRUG
Non Proprietary Name .ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20060523
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name .ALPHA.-KETOGLUTARIC ACID; ALPHA LIPOIC ACID; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BLACK COHOSH; BRYONIA ALBA ROOT; CALCITONIN HUMAN; CHLORINE; COLCHICUM AUTUMNALE BULB; NADIDE; NERVE GROWTH FACTOR; PRASTERONE; QUINHYDRONE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA FLOWER; STRONTIUM CARBONATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA ARTERY; SUS SCROFA CARTILAGE; SUS SCROFA CONJUNCTIVA; SUS SCROFA PARATHYROID GLAND; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOXICO
Strength Number 3; 3; 3; 3; 6; 6; 6; 6; 6; 3; 4; 6; 3; 3; 6; 6; 3; 6; 6; 6; 6; 6; 6; 6; 6; 6; 4
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_C]/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_C]/30mL
Pharmaceutical Classes

Complete Information of GUNA-ARTHRO


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