FDA.reportPublic FDA data

GUNA-MATRIX

Manufacturer
Guna spa
Effective date
2026-06-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-06-13 05:10:05

Label at a glance#

ProductGUNA-MATRIX
Active ingredientASCORBIC 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
Label structure10 sections

Indications and uses

Temporary Relief of general symptoms and inflammatory symptoms related to excess toxin buildup, such as: Fatigue Occasional muscle aches and pains Skin rashes Swelling

Dosage and administration

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 consult a physician

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

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



SODIUM SULFATE 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

OTC - PURPOSE SECTION

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

  • Fatigue
  • Occasional muscle aches and pains
  • Skin rashes
  • Swelling

WARNINGS

WARNINGS SECTION

  • 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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a doctor before use

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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 consult a physician

QUESTIONS

OTC - QUESTIONS SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%.

INDICATIONS & USAGE SECTION

Take 15 minutes before meals

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USMAT5USMAT

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USMAT5USMAT.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
980b5d64-e8e5-e1c9-b721-75e08f4e00a1Product name220200323
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
86ca2ee7-106a-420e-9137-a9ec1af5dbc1Product name120170110
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-416-182020-03-13C16284748780-19d75b9d1-23b8-f424-e053-dadaa90a57ceGUNA-MATRIX
17089-416-182020-03-13C16284748780-19d75b9d1-23b8-f424-e053-dadaa90a57ceGUNA-MATRIX
17089-416-182020-01-31C16284748780-19d75b9d1-23b8-f424-e053-dadaa90a57ceGUNA-MATRIX
17089-416-182020-01-31C16284748780-19d75b9d1-23b8-f424-e053-dadaa90a57ceGUNA-MATRIX

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASCORBIC ACIDACTIVE INGREDIENTPQ6CK8PD0R1
DODECAHYDROXYCYCLOHEXANE DIHYDRATEACTIVE INGREDIENT5BWD2J7B4W1
FUCUS VESICULOSUSACTIVE INGREDIENT535G2ABX9M1
HISTIDINE MONOHYDROCHLORIDEACTIVE INGREDIENT1D5Q932XM61
HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED)ACTIVE INGREDIENT92QVL9080Y1
HYALURONIDASEACTIVE INGREDIENT8KOG53Z5EM1
LACTIC ACID, DL-ACTIVE INGREDIENT3B8D35Y7S41
MALIC ACIDACTIVE INGREDIENT817L1N4CKP1
NADIDEACTIVE INGREDIENT0U46U6E8UK1
PHENYLALANINEACTIVE INGREDIENT47E5O17Y3R1
PRASTERONEACTIVE INGREDIENT459AG36T1B1
PROLACTINACTIVE INGREDIENT2S58538ZG21
RANCID BEEFACTIVE INGREDIENT29SUH5R3HU1
SODIUM DIETHYL OXALACETATEACTIVE INGREDIENT6CA025Y4FG1
SODIUM PYRUVATEACTIVE INGREDIENTPOD38AIF081
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21J1
SUS SCROFA CONJUNCTIVAACTIVE INGREDIENTW61ME6Q7171
SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLEACTIVE INGREDIENT308LM01C721
THUJA OCCIDENTALIS TWIGACTIVE INGREDIENT1NT28V93971
TYROSINEACTIVE INGREDIENT42HK56048U1
ASCORBIC ACIDACTIVE MOIETYPQ6CK8PD0R1
DIETHYL OXALACETATEACTIVE MOIETY15S56468G71
DODECAHYDROXYCYCLOHEXANEACTIVE MOIETYI1Z9VS3H641
FUCUS VESICULOSUSACTIVE MOIETY535G2ABX9M1
HISTIDINEACTIVE MOIETY4QD397987E1
HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED)ACTIVE MOIETY92QVL9080Y1
HYALURONIDASEACTIVE MOIETY8KOG53Z5EM1
LACTIC ACID, DL-ACTIVE MOIETY3B8D35Y7S41
MALIC ACIDACTIVE MOIETY817L1N4CKP1
NADIDEACTIVE MOIETY0U46U6E8UK1
PHENYLALANINEACTIVE MOIETY47E5O17Y3R1
PRASTERONEACTIVE MOIETY459AG36T1B1
PROLACTINACTIVE MOIETY2S58538ZG21
PYRUVIC ACIDACTIVE MOIETY8558G7RUTR1
RANCID BEEFACTIVE MOIETY29SUH5R3HU1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
SUS SCROFA CONJUNCTIVAACTIVE MOIETYW61ME6Q7171
SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLEACTIVE MOIETY308LM01C721
THUJA OCCIDENTALIS TWIGACTIVE MOIETY1NT28V93971
TYROSINEACTIVE MOIETY42HK56048U1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-41617089-416-18

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ASCORBIC ACIDPQ6CK8PD0RACTIB
SUS SCROFA CONJUNCTIVAW61ME6Q717ACTIB
PRASTERONE459AG36T1BACTIB
MALIC ACID817L1N4CKPACTIB
FUCUS VESICULOSUS535G2ABX9MACTIB
HISTIDINE MONOHYDROCHLORIDE1D5Q932XM6ACTIB
HYALURONIDASE8KOG53Z5EMACTIB
HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED)92QVL9080YACTIB
LACTIC ACID, DL-3B8D35Y7S4ACTIB
SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE308LM01C72ACTIB
NADIDE0U46U6E8UKACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
SODIUM PYRUVATEPOD38AIF08ACTIB
SODIUM SULFATE0YPR65R21JACTIB
PHENYLALANINE47E5O17Y3RACTIB
PROLACTIN2S58538ZG2ACTIB
RANCID BEEF29SUH5R3HUACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
DODECAHYDROXYCYCLOHEXANE DIHYDRATE5BWD2J7B4WACTIB
TYROSINE42HK56048UACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52022-11-15full-release2026-06-01 02:18:34

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GUNA-MATRIXASCORBIC 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 spafa9ed512-97dc-44a2-b32d-86ca8c2405322026-06-11WarningsExact identifier
ndc (package): 17089-416-18
ndc (product): 17089-416
ndc11 (package): 17089041618
spl id: 53f5a156-3403-726e-e063-6394a90a1111
spl set id: fa9ed512-97dc-44a2-b32d-86ca8c240532

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.