Ear Discomfort

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2021-12-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:21:50

Label at a glance#

ProductEar Discomfort
Active ingredientACONITUM NAPELLUS, BACILLUS ANTHRACIS IMMUNOSERUM RABBIT, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, CAPSICUM, MATRICARIA RECUTITA, DYSPHANIA AMBROSIOIDES, EUPHORBIA RESINIFERA RESIN, LACHESIS MUTA VENOM, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, MERCURIC CHLORIDE, PLANTAGO MAJOR, PULSATILLA VULGARIS, VERBASCUM THAPSUS
Label structure9 sections

Dosage and administration

Adults and children over 12 : Place 15 drops under the tongue up to six times per day until symptoms are relieved. Children 12 and under : Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aconitum Napellus 200C, Anthracinum 200C, Arnica Montana 200C, Baptisia Tinctoria 3X, Capsicum Annuum 6X, Chamomilla 3X, Chenopodium Anthelminticum 6X, Euphorbium Officinarum 6X, Lachesis Mutus 200C, Magnesia Phosphorica 8X, Mercurius Corrosivus 200C, Plantago Major 3X, Pulsatilla (Vulgaris) 30X, Verbascum Thapsus 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of clogging: pressure, sensitivity, or discomfort of the ear.**

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

WARNINGS:

WARNINGS SECTION

Stop use and ask a doctor if symptoms persist, there is discharge from the ear, or there is a fever.

If pregnant or breast feeding, ask a doctor before use.

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

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

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 call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Place 15 drops under the tongue up to six times per day until symptoms are relieved.

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms of clogging: pressure, sensitivity, or discomfort of the ear.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY LIDDELL LABORATORIES INC.

WOODBINE, IA 51579

WWW.LIDDELL.NET 1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL LABORATORIES

EST. 1994

26 Erd
Ear Discomfort

HOMEOPATHIC

1.0 FL. OZ. (30ml)

Ear DiscomfortEar Discomfort

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0235-12021-12-21C16284748780-19d75b9d0-6832-f424-e053-dadaa90a57ceDrug Facts:
50845-0235-12020-01-31C16284748780-19d75b9d0-6832-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-023550845-0235-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Source Document#

Source XML · Source PDF

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
c7dd57d8-36d4-4ce7-92ea-d83d8d624e5aec0ee6c7-2b09-4db7-9a82-8c1f713e694b2021-12-21WarningsExact identifier
spl id: c7dd57d8-36d4-4ce7-92ea-d83d8d624e5a
spl set id: ec0ee6c7-2b09-4db7-9a82-8c1f713e694b

Reported adverse events (FAERS/openFDA)#

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