Asthma Plus

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:55:56

Label at a glance#

ProductAsthma Plus
Active ingredientRIBES NIGRUM LEAF, VIBURNUM OPULUS BARK, QUEBRACHO BARK, BLATTA ORIENTALIS, SYMPLOCARPUS FOETIDUS ROOT, CINNAMIC ACID, GALLIC ACID, INDOLE, QUERCETIN, RUTIN, ARSENIC TRIIODIDE, NAPHTHALENE, COUMARIN, OXYGEN, DERMATOPHAGOIDES FARINAE, MALVIN
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 3 times a day or as directed by a 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

Ribes Nigrum 3X, Viburnum Opulus 3X, Quebracho 5X, Blatta Orientalis 6X, Pothos Foetidus 6X, Cinnamic Acid 6X, 12X, 30X, 12C, 30C, Gallicum Acidum 6X, 12X, 30X, 12C, 30C, Indolum 6X, 12X, 30X, 12C, 30C, Quercetin 6X, 12X, 30X, 12C, 30C, Rutin 6X, 12X, 30X, 12C, 30C, Arsenicum Iodatum 8X, Naphthalinum 8X, Coumarinum 8X, 12X, 30X, 12C, 30C, Oxygenium 12X, House Dust Mite 9C, 12C, 15C, 30C, Malvin 12C, 30C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to asthma including coughing and wheezing.**

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

WARNINGS:

WARNINGS SECTION

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

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

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to asthma including coughing and wheezing.**

**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

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-1529-1

HOMEOPATHIC

ASTHMA
PLUS

1 FL OZ (30 ml)

Asthma PlusAsthma Plus

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1529ASTHMA PLUS (RIBES NIGRUM, VIBURNUM OPULUS, QUEBRACHO, BLATTA ORIENTALIS, POTHOS FOETIDUS, CINNAMIC ACID, GALLICUM ACIDUM, INDOLUM, QUERCETIN, RUTIN, ARSENICUM IODATUM, NAPHTHALINUM, COUMARINUM, HOUSE DUST MITE, OXYGENIUM, MALVIN) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210121_d093dcae-07de-43a4-885f-c1f7d4e0e9ce.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-152943742-1529-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
ba3ba8fa-182f-4597-9a9c-b33399a13626d093dcae-07de-43a4-885f-c1f7d4e0e9ce2021-01-20WarningsExact identifier
spl id: ba3ba8fa-182f-4597-9a9c-b33399a13626
spl set id: d093dcae-07de-43a4-885f-c1f7d4e0e9ce

Reported adverse events (FAERS/openFDA)#

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