Mucous Membrane Core Formula

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:41:09

Label at a glance#

ProductMucous Membrane Core Formula
Active ingredientCEANOTHUS AMERICANUS LEAF, VERATRUM ALBUM ROOT, SEMECARPUS ANACARDIUM JUICE, SILVER NITRATE, MARSDENIA CONDURANGO BARK, GOLDENSEAL, MOMORDICA BALSAMINA IMMATURE FRUIT, OXALIS ACETOSELLA LEAF, PULSATILLA VULGARIS, SUS SCROFA BILE DUCT, SUS SCROFA COLON, SUS SCROFA DUODENUM, SUS SCROFA ESOPHAGUS, SUS SCROFA EYE, SUS SCROFA GALLBLADDER, SUS SCROFA ILEUM, PORK INTESTINE, IPECAC, SUS SCROFA JEJUNUM, POTASSIUM DICHROMATE, SUS SCROFA LUNG, SUS SCROFA NASAL MUCOSA, SODIUM DIETHYL OXALACETATE, SUS SCROFA ORAL MUCOSA, SUS SCROFA PANCREAS, PHOSPHORUS, SUS SCROFA RECTAL MUCOSA, SUS SCROFA STOMACH, SULFUR, YEAST MANNAN, WOOD CREOSOTE, LACHESIS MUTA VENOM, MANDRAGORA OFFICINARUM ROOT, SUS SCROFA URINARY BLADDER, SHIGELLA DYSENTERIAE
Label structure9 sections

Dosage and administration

Adults 3 to 10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Ceanothus Americanus 4X, Veratrum Album 4X, Anacardium Orientale 6X, Argentum Nitricum 6X, Condurango 6X, Hydrastis Canadensis 6X, Momordica Balsamina 6X, Oxalis Acetosella 6X, Pulsatilla (Vulgaris) 6X, Bile Duct (Suis) 8X, Colon (Suis) 8X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Eye (Suis) 8X, Gallbladder (Suis) 8X, Ileum (Suis) 8X, Intestine (Suis) 8X, Ipecacuanha 8X, Jejunum (Suis) 8X, Kali Bichromicum 8X, Lung, (Suis) 8X, Mucosa Nasalis Suis 8X, Natrum Oxalaceticum 8X, Oral Mucosa (Suis) 8X, Pancreas Suis 8X, Phosphorus 8X, Rectal Mucosa (Suis) 8X, Stomach (Suis) 8X, Sulphur 8X, Mannan 8X, 30X, 200X, Kreosotum 10X, Lachesis Mutus 10X, Mandragora Officinarum 10X, Urinary Bladder (Suis) 6C, Dysentery Bacillus 30C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

Temporary relief of symptoms related to congestion of the many mucous membranes of the body including GI disturbance, chronic allergies, and anxieties.**


**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult 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 tamper evident seal is broken or missing.
Store at room temperature.
Keep out of direct sunlight.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults 3 to 10 drops under the tongue 3 times daily or as directed by your health professional.
Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

Temporary relief of symptoms related to congestion of the many mucous membranes of the body including GI disturbance, chronic allergies, and anxieties.**


**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

DISTRIBUTED BY:
Deseret Biologicals, Inc., Sandy, UT 84070
800.827.9529 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUES
NAET
NDC 43742-0829-1

HOMEOPATHIC
MUCOUS MEMBRANE
Core Formula

Net Contents 1 FL OZ (30 ML)
DESBIO

Mucous Membrane Core FormulaMucous Membrane Core Formula

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-109243742-1092-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
eea500ad-00aa-4736-b261-f0232778c9ff120aab71-db2f-4dc1-9ebc-ab6def0fc3fd2018-12-14WarningsExact identifier
spl id: eea500ad-00aa-4736-b261-f0232778c9ff
spl set id: 120aab71-db2f-4dc1-9ebc-ab6def0fc3fd

Reported adverse events (FAERS/openFDA)#

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