Gasalia

Manufacturer
Laboratoires Boiron | Boiron Inc. | Boiron
Effective date
2023-05-10
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:21:09

Label at a glance#

ProductGasalia
Active ingredientACTIVATED CHARCOAL, LYCOPODIUM CLAVATUM SPORE, NUTMEG, DAIKON
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients** (in each tablet)

Carbo vegetabilis 6C HPUS (0.63 mg)

Lycopodium clavatum 6C HPUS (0.63 mg)

Nux moschata 6C HPUS (0.63 mg)

Raphanus sativus 6C HPUS (0.6 mg)

The letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Carbo vegetabilis 6C HPUS ...Relieves stomach bloating with gas

Lycopodium clavatum 6C HPUS ... Relieves bloated lower abdomen

Nux moschata 6C HPUS... Relieves abdominal bloating accompanied by constipation

Raphanus sativus 6C HPUS... Relieves abdominal pain and bloating with difficulty passing gas

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves bloating, pressure, discomfort, and pain commonly referred to as gas

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist continuously for more than 7 days or worsen.

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: At the onset of symptoms, dissolve 2 tablets in the mouth every hour until symptoms are relieved. If necessary, dissolve 2 tablets in the mouth 15 minutes before meals. Children under 6 years of age: Ask a doctor.

SPL UNCLASSIFIED SECTION

do not use if glued carton and flaps are open or if the blister seal is broken.

store below 86°F (30° C)

Plant-Powered Relief

No Known Drug Interactions

60 Meltaway Tablets

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

**C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

INACTIVE INGREDIENT SECTION

croscarmellose sodium, lactose, magnesium stearate.

OTC - QUESTIONS SECTION

Questions or comments?
BoironUSA.com
Info@Boiron.com
1-800-BOIRON-1
(1-800-264-7661)

Distributed by Boiron, Inc.

Newtown Square, PA 19073

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabellabellabel68898836889883boxbox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9134-042023-01-31C16284748780-1f386c649-a5d8-0266-e053-dadaa90a7c1aGasalia
0220-9134-042023-01-30C16284748780-1f386c649-a5d8-0266-e053-dadaa90a7c1aGasalia

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9134-04Gasalia60 in 1 BLISTER PACKTABLET608

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9134GASALIA (ACTIVATED CHARCOAL, LYCOPODIUM CLAVATUM SPORE, NUTMEG, DAIKON) TABLET [LABORATOIRES BOIRON]8Current NDC, Legacy NDC, 1 package rows20230511_3f93dfdc-8edb-4e4b-a571-4cd202e02113.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H103
DAIKONACTIVE INGREDIENT86R5J6D01D3
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4793
NUTMEGACTIVE INGREDIENTAEE24M3MQ93
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H103
DAIKONACTIVE MOIETY86R5J6D01D3
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4793
NUTMEGACTIVE MOIETYAEE24M3MQ93
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH483
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I303

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-91340220-9134-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

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 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / ORAL736 mgExact identifier — unii+route+dosage form
2 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
GasaliaACTIVATED CHARCOAL, LYCOPODIUM CLAVATUM SPORE, NUTMEG, DAIKONLaboratoires Boiron3f93dfdc-8edb-4e4b-a571-4cd202e021132023-05-10Exact identifier
ndc (package): 0220-9134-04
ndc (product): 0220-9134
ndc11 (package): 00220913404
spl id: fb5cf5e0-86d4-3f5a-e053-6294a90a2d38
spl set id: 3f93dfdc-8edb-4e4b-a571-4cd202e02113

Reported adverse events (FAERS/openFDA)#

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