MBM 5 Large Intestine

Manufacturer
The Wellness Center | Apotheca Company
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:55

Label at a glance#

ProductMBM 5 Large Intestine
Active ingredientSUS SCROFA COLON, GOLDENSEAL, SENNA LEAF, COPPER, NITRIC ACID, AMANITA MUSCARIA FRUITING BODY, ARNICA MONTANA WHOLE, BAPTISIA TINCTORIA WHOLE
Label structure9 sections

Dosage and administration

Feel the emotion fully, breathe deeply-connected breaths. Put 5 drops under tongue to release emotion. Continue 5 drops 2 times daily as needed. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Colon (Suis) 3C, Hydrastis Canadensis 3C, Senna (Cassia Angustifolia) 3C, Cuprum Metallicum 89C, 144C, Nitricum Acidum 89C, 233C, Agaricus Muscarius 144C, Arnica Montana 144C, Baptisia Tinctoria 144C.

INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of feelings of being stuck.

WARNINGS:

WARNINGS SECTION

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. Do not use if seal is broken or missing.

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.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Feel the emotion fully, breathe deeply-connected breaths. Put 5 drops under tongue to release emotion. Continue 5 drops 2 times daily as needed. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of feelings of being stuck.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Organic Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

MFD FOR: The Wellness Center

for Research and Education, Inc.

1237 S. Victoria Ave., Suite 169

Oxnard, CA 93035

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Theresa Dale's

MIND BODY MERIDIAN

NDC: 50181-0083-1

Fibonacci Series

5

Large

Intestine

Stuck

HOMEOPATHIC

1 fluid oz. (30 ml)

MBM 5 Large IntestineMBM 5 Large Intestine

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0083-12025-06-06C16284748780-11030e365-4203-111a-e063-dadaa90a10e2DRUG FACTS:
50181-0083-12024-01-30C16284748780-11030e365-4203-111a-e063-dadaa90a10e2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50181-0083-1MBM 5 Large Intestine30 mL in 1 BOTTLE, DROPPERLIQUID302

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50181-008350181-0083-1

Ingredients#

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

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

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
MBM 5 Large IntestineCOLON (SUIS), HYDRASTIS CANADENSIS, SENNA (CASSIA ANGUSTIFOLIA), CUPRUM METALLICUM, NITRICUM ACIDUM, AGARICUS MUSCARIUS, ARNICA MONTANA, BAPTISIA TINCTORIAThe Wellness Center0804f33c-28d8-4d5d-8002-36e1daa6cca32025-06-06WarningsExact identifier
ndc (package): 50181-0083-1
ndc (product): 50181-0083
ndc11 (package): 50181008301
spl id: f32cd563-3bc2-4003-8b7f-0a3d785bafab
spl set id: 0804f33c-28d8-4d5d-8002-36e1daa6cca3

Reported adverse events (FAERS/openFDA)#

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