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GUNA-MATRIX - 17089-416-18 - (ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - P)

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Drug Information of GUNA-MATRIX

Product NDC: 17089-416
Proprietary Name: GUNA-MATRIX
Non Proprietary Name: ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - P
Active Ingredient(s): 4; 6; 4; 4; 4; 6; 4; 6; 6; 4; 6; 6; 12; 6; 6; 12; 6; 6; 12; 4    [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 & nbsp;   ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - P
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of GUNA-MATRIX

Product NDC: 17089-416
Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100527

Package Information of GUNA-MATRIX

Package NDC: 17089-416-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX (17089-416-18) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of GUNA-MATRIX

NDC Code 17089-416-18
Proprietary Name GUNA-MATRIX
Package Description 1 BOTTLE, DROPPER in 1 BOX (17089-416-18) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 17089-416
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - P
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20100527
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Guna spa
Substance Name ASCORBIC ACID; DODECAHYDROXYCYCLOHEXANE DIHYDRATE; FUCUS VESICULOSUS; HISTIDINE MONOHYDROCHLORIDE; HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED); HYALURONIDASE; LACTIC ACID, DL-; MALIC ACID; NADIDE; PHENYLALANINE; PRASTERONE; PROLACTIN; RANCID BEEF; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SODIUM SULFATE; SUS SCROFA CONJUNCTIVA; SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE; THUJA OCCIDENTALIS TWIG; TYROSINE
Strength Number 4; 6; 4; 4; 4; 6; 4; 6; 6; 4; 6; 6; 12; 6; 6; 12; 6; 6; 12; 4
Strength Unit [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
Pharmaceutical Classes

Complete Information of GUNA-MATRIX


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