FDA.reportPublic FDA data

Drug Facts

Manufacturer
The Wise Alternative | Apotheca Company
Effective date
2026-08-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-08-07 01:00:58

Label at a glance#

ProductGluten Sensitivity Formula
Active ingredientLYCOPODIUM CLAVATUM SPORE, PULSATILLA VULGARIS
Label structure9 sections

Indications and uses

For temporary relief of symptoms associated with constipation, bloating, diarrhea and othe symptoms of poor digetsion.

Dosage and administration

Adults take 6 capsules one time daily. Children under 30 lbs take 2 capsules one time daily, up to 60 lbs take 3 capsules one time daily, up to 90 lbs take 4 capsules one time daily. Can take capsule apart and mix powder in juice. Consult a physician for ude in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Lycopodium Clavatum 12X, Pulsatilla 12X

INDICATIONS

OTC - PURPOSE SECTION

For temporary relief of symptoms associated with constipation, bloating, diarrhea and othe symptoms of poor digetsion.

WARNINGS

WARNINGS SECTION

If pregnant or breastfeeding, ask a health professional before use. If you have allergy to fish (including Salmon), you should not use this product. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is borken or missing. Store in a cool, dry place.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults take 6 capsules one time daily. Children under 30 lbs take 2 capsules one time daily, up to 60 lbs take 3 capsules one time daily, up to 90 lbs take 4 capsules one time daily. Can take capsule apart and mix powder in juice. Consult a physician for ude in children under 12 years of age.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aronia (berry), Capsule (Gelatin), DNA (Deoxyribonucleic acidum sodium salt), Folic Acid, L-Carnosine, Rice Flour, RNA (Ribonucleic acid sodium salt), Vitamin D3 (from Cholecalciferol)

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

For temporary relief of symptoms associated with constipation, bloating, diarrhea and othe symptoms of poor digetsion.

QUESTIONS

OTC - QUESTIONS SECTION

Distributed by: The Wise Alternative

6572 E. 24th Street

Tulsa, OK 74129

(918) 896-0665

www.thewisealternative.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Wise Alternative

Gluten Sensitivity Formula

Homeopathic 180 Capsules

Gluten Sensitivity FormulaGluten Sensitivity Formula

Gluten Sensitivity FormulaGluten Sensitivity Formula

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51096-0001-12020-01-31C16284748780-19d75b9d0-6abd-f424-e053-dadaa90a57ceDrug Facts
51096-0001-12020-01-31C16284748780-19d75b9d0-6abd-f424-e053-dadaa90a57ceDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
ARONIA MELANOCARPA FRUITINACTIVE INGREDIENTS935718Z2Q1
BROWN RICEINACTIVE INGREDIENT659G217HPG1
CARNOSINEINACTIVE INGREDIENT8HO6PVN24W1
CHOLECALCIFEROLINACTIVE INGREDIENT1C6V77QF411
CYBERLINDNERA JADINII RNAINACTIVE INGREDIENT5620EH64M41
FOLIC ACIDINACTIVE INGREDIENT935E97BOY81
GELATININACTIVE INGREDIENT2G86QN327L1
ONCORHYNCHUS MASOU SPERM DNAINACTIVE INGREDIENT1SI16O1B9R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51096-000151096-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
ARONIA MELANOCARPA FRUITS935718Z2QIACT
GELATIN2G86QN327LIACT
ONCORHYNCHUS MASOU SPERM DNA1SI16O1B9RIACT
FOLIC ACID935E97BOY8IACT
CARNOSINE8HO6PVN24WIACT
BROWN RICE659G217HPGIACT
CYBERLINDNERA JADINII RNA5620EH64M4IACT
CHOLECALCIFEROL1C6V77QF41IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12013-03-05full-release2026-06-01 02:04:48

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GELATINGELATIN2G86QN327LCAPSULE / ORAL10932 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GELATINGELATIN2G86QN327LCAPSULE / ORAL10932 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
Gluten Sensitivity FormulaLYCOPODIUM CLAVATUM, PULSATILLAThe Wise Alternative42b2d54a-5e02-44ed-8172-a45c5addf7c22026-08-04WarningsExact identifier
ndc (package): 51096-0001-1
ndc (product): 51096-0001
ndc11 (package): 51096000101
spl id: 04a36afe-0f09-47fe-8d8d-ad77bf658ee4
spl set id: 42b2d54a-5e02-44ed-8172-a45c5addf7c2

Reported adverse events (FAERS/openFDA)#

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