FDA.reportPublic FDA data

GUNA-BOWEL

Manufacturer
Guna spa
Effective date
2026-06-10
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-06-12 05:10:06

Label at a glance#

ProductGUNA-BOWEL
Active ingredientALOE, ALUMINUM OXIDE, BRYONIA ALBA ROOT, SILYBUM MARIANUM SEED, CHELIDONIUM MAJUS, CHOLECALCIFEROL, COLLINSONIA, SUS SCROFA COLON, POTASSIUM CARBONATE, SODIUM CARBONATE, NIACIN, STRYCHNOS NUX-VOMICA SEED, PANTOTHENIC ACID, SUS SCROFA RECTUM, FRANGULA ALNUS BARK, RHUBARB, SKATOLE, TARAXACUM OFFICINALE, THIAMINE
Label structure10 sections

Indications and uses

Temporary relief of symptoms due to constipation: Abdominal bloating Abdominal discomfort Irregularity of bowel movements

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 5 drops in a glass of water, consult a physician

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

ALOE SOCOTRINA 2X LAXATIVE

ALUMINA 6X 8X CONSTIPATION

BRYONIA ALBA 6X 8X SPASMOLYTIC

CARDUUS MARIANUS 2X SUPPORTS DIGESTION

CHELIDONIUM MAJUS 2X SUPPORTS DIGESTION

CHOLECALCIFEROL 2X ANTIOXIDANT

COLLINSONIA CANADENSIS 2X HEMORRHOIDS

COLON 6X 12X 30X STIMULATES DIGESTION

KALI CARBONICUM 6X 8X 12X BACK PAIN

NATRUM CARBONICUM 6X 8X 12X BLOATING AFTER EATING

NIACIN 2X REGULATES CHOLESTEROL

NUX VOMICA 6X 8X HELPS DIGESTION

PANTOTHENIC ACID 2X STIMULATES DIGESTION

RECTUM 6X 12X 30X STIMULATES DIGESTION

RHAMNUS FRANGULA 2X LAXATIVE

RHEUM 2X LAXATIVE

SKATOLUM 6X 10X LAXATIVE

TARAXACUM 2X LAXATIVE

THIAMINUM HYDROCHLORICUM 4X STIMULATES DIGESTION


USES

OTC - PURPOSE SECTION

Temporary relief of symptoms due to constipation:

  • Abdominal bloating
  • Abdominal discomfort
  • Irregularity of bowel movements

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 5 drops in a glass of water, consult a physician

QUESTIONS

OTC - QUESTIONS SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol

INDICATIONS & USAGE SECTION

Take 15 minutes before meals

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USBOW-rEV055USBOW-rEV05

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USBOW5USBOW-Rev05.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
e2dae634-14ed-febf-08ee-93196433b5b7Product name920190614
0a5e5249-329b-0cff-e714-77159f193a87Product name120140508
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508
6b7a6f32-42a6-994d-5ab6-d180e92ee9d8Product name120140508
d394f843-7479-dc48-dbd3-232266c5548cProduct name120140508
dc9a5fb6-14e2-1cc8-a567-a781fd1f0212Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17089-293-182020-03-13C16284748780-19d75b9d0-a129-f424-e053-dadaa90a57ceGUNA-BOWEL
17089-293-182020-03-13C16284748780-19d75b9d0-a129-f424-e053-dadaa90a57ceGUNA-BOWEL
17089-293-182020-01-31C16284748780-19d75b9d0-a129-f424-e053-dadaa90a57ceGUNA-BOWEL
17089-293-182020-01-31C16284748780-19d75b9d0-a129-f424-e053-dadaa90a57ceGUNA-BOWEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALOEACTIVE INGREDIENTV5VD430YW92
ALUMINUM OXIDEACTIVE INGREDIENTLMI26O69332
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B2
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNN2
CHOLECALCIFEROLACTIVE INGREDIENT1C6V77QF412
COLLINSONIAACTIVE INGREDIENTJ9BTD5377V2
FRANGULA ALNUS BARKACTIVE INGREDIENTS2D77IH61R2
NIACINACTIVE INGREDIENT2679MF687A2
PANTOTHENIC ACIDACTIVE INGREDIENT19F5HK27372
POTASSIUM CARBONATEACTIVE INGREDIENTBQN1B9B9HA2
RHUBARBACTIVE INGREDIENTG280W4MW6E2
SILYBUM MARIANUM SEEDACTIVE INGREDIENTU946SH95EE2
SKATOLEACTIVE INGREDIENT9W945B5H7R2
SODIUM CARBONATEACTIVE INGREDIENT45P3261C7T2
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139192
SUS SCROFA COLONACTIVE INGREDIENT94J255A0UC2
SUS SCROFA RECTUMACTIVE INGREDIENTQV1358E70N2
TARAXACUM OFFICINALEACTIVE INGREDIENT39981FM3752
THIAMINEACTIVE INGREDIENTX66NSO3N352
ALOEACTIVE MOIETYV5VD430YW92
ALUMINUM OXIDEACTIVE MOIETYLMI26O69332
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B2
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNN2
CHOLECALCIFEROLACTIVE MOIETY1C6V77QF412
COLLINSONIAACTIVE MOIETYJ9BTD5377V2
FRANGULA ALNUS BARKACTIVE MOIETYS2D77IH61R2
NIACINACTIVE MOIETY2679MF687A2
PANTOTHENIC ACIDACTIVE MOIETY19F5HK27372
POTASSIUM CATIONACTIVE MOIETY295O53K1522
RHUBARBACTIVE MOIETYG280W4MW6E2
SILYBUM MARIANUM SEEDACTIVE MOIETYU946SH95EE2
SKATOLEACTIVE MOIETY9W945B5H7R2
SODIUM CATIONACTIVE MOIETYLYR4M0NH372
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139192
SUS SCROFA COLONACTIVE MOIETY94J255A0UC2
SUS SCROFA RECTUMACTIVE MOIETYQV1358E70N2
TARAXACUM OFFICINALEACTIVE MOIETY39981FM3752
THIAMINEACTIVE MOIETYX66NSO3N352
ALCOHOLINACTIVE INGREDIENT3K9958V90M2

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-29317089-293-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ALOEV5VD430YW9ACTIB
ALUMINUM OXIDELMI26O6933ACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SILYBUM MARIANUM SEEDU946SH95EEACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
CHOLECALCIFEROL1C6V77QF41ACTIB
COLLINSONIAJ9BTD5377VACTIB
SUS SCROFA COLON94J255A0UCACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
SODIUM CARBONATE45P3261C7TACTIB
NIACIN2679MF687AACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PANTOTHENIC ACID19F5HK2737ACTIB
SUS SCROFA RECTUMQV1358E70NACTIB
FRANGULA ALNUS BARKS2D77IH61RACTIB
RHUBARBG280W4MW6EACTIB
SKATOLE9W945B5H7RACTIB
TARAXACUM OFFICINALE39981FM375ACTIB
THIAMINEX66NSO3N35ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62022-11-14full-release2026-06-01 02:18:31

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
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact 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
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact 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
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii+route
22 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact 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-BOWELALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA RECTUM - TARAXACUM OFFICINALE - THIAMINE -Guna spa75465821-a889-4697-b470-e9588a5232052026-06-10WarningsExact identifier
ndc (package): 17089-293-18
ndc (product): 17089-293
ndc11 (package): 17089029318
spl id: 53e95cf4-56b0-8501-e063-6294a90a3edd
spl set id: 75465821-a889-4697-b470-e9588a523205

Reported adverse events (FAERS/openFDA)#

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