Label: 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 - solution/ drops

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 21, 2018

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS/PURPOSE

    ASCORBIC ACID 4X ANTIOXIDANT

    CONJUNCTIVA TISSUE 6X DETOXIFICATION

    DEHYDROEPIANDROSTERON 6X HORMONAL SUPPORT

    DL-MALIC ACID 6X PROMOTE CELL METABOLISM

    FUCUS VESICULOSUS 4X DETOXIFICATION

    HISTIDINE 4X ANTI-INFLAMMATORY

    HYALURONIDASE 6X ANTI-INFLAMMATORY

    INTERLEUKIN 6 4C IMMUNE SUPPORT

    LACTICUM ACIDUM 4X ANTIOXIDANT

    LYMPHATIC VESSEL 6X IMMUNE SUPPORT

    NADIDUM 6X METABOLIC SUPPORT

    NATRUM OXALACETICUM 6X ANTIOXIDANT

    NATRUM PYRUVICUM 6X ANTIOXIDANT

    NATRUM SULPHURICUM 6X, 8X, 12X, 30X, 200X ANTIOXIDANT

    PHENYLALANINE 4X IMPROVE CONCENTRATION

    PROLACTIN 6X IMPROVE CONCENTRATION

    PYROGENIUM 12X ANTI-INFLAMMATORY

    THUJA OCCIDENTALIS 6X, 8X, 12X, 30X, 200X DETOXIFICATION

    TRICHINOYL PHOSPHATE 6X ANTIOXIDANT

    TYROSINE 4X IMMUNE SUPPORT

  • USES

    Temporary Relief of general symptoms and inflammatory symptoms related to excess toxin buildup, such as:

    • Fatigue
    • Occasionale muscle aches and pains
    • Skin rashes
    • Swelling
  • WARNINGS

    • Stop use and ask doctor if symptoms persist more than 5 days.
    • If pregnant or breast-feeding ask a health professional before use.
    • Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
    • Contains ethyl alcohol 30%
  • PREGNANCY

    If pregnant or breast-feeding ask a doctor before use

  • WARNINGS

    Keep out of reach of children

  • DIRECTIONS

    Adults and children 12 years and older 20 drops in a little water 2 times per day

    Children between 12 years and 6 years of age 10 drops in a little water 2 times per day

    Children under 6 years 5 drops in a little water 2 times per day

  • QUESTIONS

    Questions?: info@gunainc.com
    Tel. (484) 223-3500

  • INACTIVE INGREDIENT

    Inactive ingredient: Ethyl alcohol 30%.

  • INDICATIONS & USAGE

    Take 15 minutes before meals

  • PRINCIPAL DISPLAY PANEL

    5USMAT-REV04-07-05-18

  • INGREDIENTS AND APPEARANCE
    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 - solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17089-416
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID4 [hp_X]  in 30 mL
    SUS SCROFA CONJUNCTIVA (UNII: W61ME6Q717) (SUS SCROFA CONJUNCTIVA - UNII:W61ME6Q717) SUS SCROFA CONJUNCTIVA6 [hp_X]  in 30 mL
    PRASTERONE (UNII: 459AG36T1B) (PRASTERONE - UNII:459AG36T1B) PRASTERONE6 [hp_X]  in 30 mL
    MALIC ACID (UNII: 817L1N4CKP) (MALIC ACID - UNII:817L1N4CKP) MALIC ACID6 [hp_X]  in 30 mL
    FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS4 [hp_X]  in 30 mL
    HISTIDINE MONOHYDROCHLORIDE (UNII: 1D5Q932XM6) (HISTIDINE - UNII:4QD397987E) HISTIDINE MONOHYDROCHLORIDE4 [hp_X]  in 30 mL
    HYALURONIDASE (UNII: 8KOG53Z5EM) (HYALURONIDASE - UNII:8KOG53Z5EM) HYALURONIDASE6 [hp_X]  in 30 mL
    HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) (UNII: 92QVL9080Y) (HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - UNII:92QVL9080Y) HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED)4 [hp_C]  in 30 mL
    LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (LACTIC ACID, DL- - UNII:3B8D35Y7S4) LACTIC ACID, DL-4 [hp_X]  in 30 mL
    SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72) (SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - UNII:308LM01C72) SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE6 [hp_X]  in 30 mL
    NADIDE (UNII: 0U46U6E8UK) (NADIDE - UNII:0U46U6E8UK) NADIDE6 [hp_X]  in 30 mL
    SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG) (DIETHYL OXALACETATE - UNII:15S56468G7) SODIUM DIETHYL OXALACETATE6 [hp_X]  in 30 mL
    SODIUM PYRUVATE (UNII: POD38AIF08) (PYRUVIC ACID - UNII:8558G7RUTR) SODIUM PYRUVATE6 [hp_X]  in 30 mL
    SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM SULFATE12 [hp_X]  in 30 mL
    PHENYLALANINE (UNII: 47E5O17Y3R) (PHENYLALANINE - UNII:47E5O17Y3R) PHENYLALANINE4 [hp_X]  in 30 mL
    PROLACTIN (UNII: 2S58538ZG2) (PROLACTIN - UNII:2S58538ZG2) PROLACTIN6 [hp_X]  in 30 mL
    RANCID BEEF (UNII: 29SUH5R3HU) (RANCID BEEF - UNII:29SUH5R3HU) RANCID BEEF12 [hp_X]  in 30 mL
    THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG12 [hp_X]  in 30 mL
    DODECAHYDROXYCYCLOHEXANE DIHYDRATE (UNII: 5BWD2J7B4W) (DODECAHYDROXYCYCLOHEXANE - UNII:I1Z9VS3H64) DODECAHYDROXYCYCLOHEXANE DIHYDRATE6 [hp_X]  in 30 mL
    TYROSINE (UNII: 42HK56048U) (TYROSINE - UNII:42HK56048U) TYROSINE4 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 9 mL  in 30 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17089-416-181 in 1 BOX12/21/2018
    130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/27/2010
    Labeler - Guna spa (430538264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guna spa338587646manufacture(17089-416)