FDA.reportPublic FDA data

GUNA MATRIX DETOX

Product NDC
17089-460
11-digit product format
170890460
Labeler code
17089
Product ID
17089-460_b2587436-faab-37c8-e053-2995a90a3fba
Type
HUMAN OTC DRUG
Nonproprietary name
sodium sulfate - podophyllum peltatum root - solidago virgaurea flowering top - apis mellifera - equisetum hyemale - strychnos nux vomica seed - hamamelis virginiana root bark stem bark - lycopodium clavatum spore - galium aparine whole - thuja occidentalis leafy twig - berberis vulgaris root bark - myosotis arvensis - chelidonium majus whole - fucus vesiculosus -
Dosage form
SOLUTION/ DROPS
Route
ORAL
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-07-14
Substance
CONIUM MACULATUM FLOWERING TOP; FUCUS VESICULOSUS; GALIUM APARINE WHOLE; GRAPHITE; MALIC ACID; MYOSOTIS ARVENSIS; RANCID BEEF; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SODIUM SULFATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA VEIN; THUJA OCCIDENTALIS LEAFY TWIG; URTICA URENS WHOLE
Active strength
3; 6; 4; 12; 6; 4; 12; 8; 3; 3; 12; 2; 6; 6; 6 [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
Pharmacologic classes
Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
GUNA MATRIX DETOX
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FUCUS VESICULOSUS3 [hp_X]/30mL
SUS SCROFA VEIN6 [hp_X]/30mL
GALIUM APARINE WHOLE4 [hp_X]/30mL
THUJA OCCIDENTALIS LEAFY TWIG12 [hp_X]/30mL
CONIUM MACULATUM FLOWERING TOP6 [hp_X]/30mL
MYOSOTIS ARVENSIS4 [hp_X]/30mL
SODIUM PYRUVATE12 [hp_X]/30mL
MALIC ACID8 [hp_X]/30mL
GRAPHITE3 [hp_X]/30mL
SILICON DIOXIDE3 [hp_X]/30mL
SODIUM SULFATE12 [hp_X]/30mL
SODIUM DIETHYL OXALACETATE2 [hp_X]/30mL
SOLIDAGO VIRGAUREA FLOWERING TOP6 [hp_X]/30mL
URTICA URENS WHOLE6 [hp_X]/30mL
RANCID BEEF6 [hp_X]/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 15 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
535G2ABX9MInternal UNII lookup
2510RH3I89Internal UNII lookup
Z4B6561488Internal UNII lookup
1NT28V9397Internal UNII lookup
Q28R5GF371Internal UNII lookup
C73BK97H5JInternal UNII lookup
POD38AIF08Internal UNII lookup
817L1N4CKPInternal UNII lookup
4QQN74LH4OInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
0YPR65R21JInternal UNII lookup
6CA025Y4FGInternal UNII lookup
5405K23S50Internal UNII lookup
IHN2NQ5OF9Internal UNII lookup
29SUH5R3HUInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
a369b95b-4d57-f149-e053-2995a90a87e3Available on FDA.report

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
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
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-460-18GUNA MATRIX DETOX30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS302
17089-460-18GUNA MATRIX DETOX1 in 1 BOXSOLUTION/ DROPS12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-460GUNA MATRIX DETOX (SODIUM SULFATE - PODOPHYLLUM PELTATUM ROOT - SOLIDAGO VIRGAUREA FLOWERING TOP - APIS MELLIFERA - EQUISETUM HYEMALE - STRYCHNOS NUX VOMICA SEED - HAMAMELIS VIRGINIANA ROOT BARK STEM BARK - LYCOPODIUM CLAVATUM SPORE - GALIUM APARINE WHOLE - THUJA OCCIDENTALIS LEAFY TWIG - BERBERIS VULGARIS ROOT BARK - MYOSOTIS ARVENSIS - CHELIDONIUM MAJUS WHOLE - FUCUS VESICULOSUS -) SOLUTION/ DROPS [GUNA SPA]2Current NDC, Legacy NDC, 2 package rows20201024_a369b95b-4d57-f149-e053-2995a90a87e3.zip

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 MATRIX DETOXSODIUM SULFATE - PODOPHYLLUM PELTATUM ROOT - SOLIDAGO VIRGAUREA FLOWERING TOP - APIS MELLIFERA - EQUISETUM HYEMALE - STRYCHNOS NUX VOMICA SEED - HAMAMELIS VIRGINIANA ROOT BARK STEM BARK - LYCOPODIUM CLAVATUM SPORE - GALIUM APARINE WHOLE - THUJA OCCIDENTALIS LEAFY TWIG - BERBERIS VULGARIS ROOT BARK - MYOSOTIS ARVENSIS - CHELIDONIUM MAJUS WHOLE - FUCUS VESICULOSUS -Guna spaa369b95b-4d57-f149-e053-2995a90a87e32020-10-23Warnings, Adverse reactionsExact identifier
ndc (product): 17089-460

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17089-460-18170890460181 BOTTLE, DROPPER in 1 BOX (17089-460-18) / 30 mL in 1 BOTTLE, DROPPER2020-07-140000-00-00NoNoCurrent