FDA.reportPublic FDA data

GUNA BOWEL PLUS

Manufacturer
Guna spa
Effective date
2021-01-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:10

Label at a glance#

ProductGUNA BOWEL PLUS
Active ingredientALOE, ALUMINUM OXIDE, BRYONIA ALBA ROOT, SILYBUM MARIANUM SEED, CHELIDONIUM MAJUS, ACTIVATED CHARCOAL, COLLINSONIA, SUS SCROFA PANCREAS, POTASSIUM CARBONATE, SODIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, FRANGULA ALNUS BARK, RHUBARB, SKATOLE, TARAXACUM OFFICINALE, THIAMINE
Label structure10 sections

Indications and uses

Temporary relief of gastrointestinal disorders, such as: constipation nausea abdominal gas impaired digestion

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: consulta a physician

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Take 15 minutes before meals

INACTIVE INGREDIENT SECTION

Inactive ingredient: Ethyl alcohol 30%

QUESTIONS

OTC - QUESTIONS SECTION

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

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: consulta a physician

WARNINGS

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children




PREGNANCY

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding ask a health care professional before use

WARNINGS

WARNINGS SECTION

  • Stop use and ask doctor if symptoms persist more than 5 days.
  • If pregnant or breast-feeding ask a health care professional before use.
  • Keep out of reach of children. In case of accidental overdose, seek professional assitance ot or contact a Poison Control Center immediately
  • Contains Aloe: do not use orally for more than 30 days.
  • Contains ethyl alcohol 30%

USES

OTC - PURPOSE SECTION

Temporary relief of gastrointestinal disorders, such as:

  • constipation
  • nausea
  • abdominal gas
  • impaired digestion

ACTIVE INGREDIENTS/PURPOSE

OTC - ACTIVE INGREDIENT SECTION

Aloe 4X Relieves constipation

Alumina 6X, 8X Relieves constipation

Bryonia 6X, 8X Relieves nausea, appetite disorders

Carbo vegetabilis 6X Helps digestion

Carduus marianus 2X Supports liver function

Chelidonium majus 2X Supports liver and gallbladder function

Collinsonia canadensis 2X Relieves hemorrhoids and constipation

Kali carbonicum 6X, 8X, 12X Relieves abdominal gas and nausea

Lycopodium clavatum 2X Supports liver function and drainage

Natrum carbonicum 6X, 8X, 12X Helps digestion

Nux vomica 6X, 8X Relieves abdominal gas and helps digestion

Pancreas suis 6X Relieves nausea, appetite disorders

Rhamnus frangula 2X Relieves nausea

Rheum 2X Relieves constipation

Skatolum 6X, 10X Helps digestion

Taraxacum officinale 2X Supports liver and gallbladder function

Thiaminum hydroc. 4X Relieves abdominal gas and helps digestion

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5USBOP-55USBOP-5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix5USBOP5USBOP-5.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17089-470-18GUNA BOWEL PLUS1 in 1 BOXSOLUTION/ DROPS11
17089-470-18GUNA BOWEL PLUS30 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17089-470GUNA BOWEL PLUS (ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -) SOLUTION/ DROPS [GUNA SPA]1Current NDC, Legacy NDC, 2 package rows20210117_b3aa4fd3-c87a-ccd2-e053-2995a90a46a9.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17089-47017089-470-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ALOEV5VD430YW9ACTIB
ALUMINUM OXIDELMI26O6933ACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SILYBUM MARIANUM SEEDU946SH95EEACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
COLLINSONIAJ9BTD5377VACTIB
SUS SCROFA PANCREAS9Y3J3362RYACTIB
POTASSIUM CARBONATEBQN1B9B9HAACTIB
SODIUM CARBONATE45P3261C7TACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
FRANGULA ALNUS BARKS2D77IH61RACTIB
RHUBARBG280W4MW6EACTIB
SKATOLE9W945B5H7RACTIB
TARAXACUM OFFICINALE39981FM375ACTIB
THIAMINEX66NSO3N35ACTIB

Source Document#

Source XML

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 BOWEL PLUSACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -Guna spab3aa4fd3-c87a-ccd2-e053-2995a90a46a92021-01-17WarningsExact identifier
ndc (package): 17089-470-18
ndc (product): 17089-470
ndc11 (package): 17089047018
spl id: b3aa6401-9af7-b0d5-e053-2995a90a10ef
spl set id: b3aa4fd3-c87a-ccd2-e053-2995a90a46a9

Reported adverse events (FAERS/openFDA)#

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