NDC 17089-416

GUNA-MATRIX

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 -

GUNA-MATRIX is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Ascorbic Acid; Sus Scrofa Conjunctiva; Prasterone; Malic Acid; Fucus Vesiculosus; Histidine Monohydrochloride; Hyaluronidase; Human Interleukin-6 (nonglycosylated); Lactic Acid, Dl-; Sus Scrofa Small Intestine Mucosa Lymph Follicle; Nadide; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Sodium Sulfate; Phenylalanine; Prolactin; Rancid Beef; Thuja Occidentalis Leafy Twig; Dodecahydroxycyclohexane Dihydrate; Tyrosine.

Product ID17089-416_7dc58045-2659-0579-e053-2a91aa0aa7d9
NDC17089-416
Product TypeHuman Otc Drug
Proprietary NameGUNA-MATRIX
Generic NameAscorbic 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 -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2010-05-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameASCORBIC ACID; SUS SCROFA CONJUNCTIVA; PRASTERONE; MALIC ACID; FUCUS VESICULOSUS; HISTIDINE MONOHYDROCHLORIDE; HYALURONIDASE; HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED); LACTIC ACID, DL-; SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE; NADIDE; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SODIUM SULFATE; PHENYLALANINE; PROLACTIN; RANCID BEEF; THUJA OCCIDENTALIS LEAFY TWIG; DODECAHYDROXYCYCLOHEXANE DIHYDRATE; TYROSINE
Active Ingredient Strength4 [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
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 17089-416-18

1 BOTTLE, DROPPER in 1 BOX (17089-416-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-416-18 [17089041618]

GUNA-MATRIX SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details


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