EARACHE DROPS

Manufacturer
Wal-Mart Stores, Inc
Effective date
2022-12-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:44:10

Label at a glance#

ProductEARACHE DROPS
Active ingredientATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, MATRICARIA RECUTITA, LYCOPODIUM CLAVATUM SPORE, PULSATILLA VULGARIS, SULFUR
Label structure14 sections

Indications and uses

Temporarily relieves symptoms of earache after diagnosis by a physician, including: ■ minor fever ■ ear pain or throobing ■ irritability ■ occasional sleeplessness ■ common pain or itching of "swimmer's ear"

Dosage and administration

■ Shake well before using. Adults and children ages 2 years and over: TIit head sideways and apply 3·4 drops into involved ear (tip of applicator should not enter ear canal). Keep head tilted for at least 2 minutes to keep drops in ear. Repeat until relieved, up to 4 times daily.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Temporarily relieves symptoms of earache after diagnosis by a physician, including: ■ minor fever ■ ear pain or throobing ■ irritability ■ occasional sleeplessness ■ common pain or itching of "swimmer's ear"

Drug Facts

SPL UNCLASSIFIED SECTION

OTC - ACTIVE INGREDIENT SECTION

Active ingredientsPurpose

Belladonna 30C HPUS

(less than 0.0000000000001% Alkaloids)

minor fever
Calcarea Carbonica 30C HPUSthrobbing ear pain
Chamomilla 30C HPUSoccasional sleeplessness and irritability
Lycopodium 30C HPUSear pain
Pulsatilla 30C HPUSear itching, pain worse at night
Sulphur 30C HPUSear pain with burning

"HPUS" indicates the active ingredients are in the official Homeopathic Pharmacopœia of the United States

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves symptoms of earache after diagnosis by a physician, including: ■ minor fever ■ ear pain or throobing ■ irritability ■ occasional sleeplessness ■ common pain or itching of "swimmer's ear"

Warnings

WARNINGS SECTION

Keep away from eyes. Do not take by mouth. Earache drops are only to be used in ears.

OTC - PREGNANCY OR BREAST FEEDING SECTION

As with any drug, ask a doctor before use ii pregnant or breast-reeding.

OTC - DO NOT USE SECTION

Do not use if you have ear tubes, damaged ear drums or after ear surgery.

OTC - ASK DOCTOR SECTION

Consult a physician if:

■ symptoms persist for more than 48 hours or wcraen.
■ discharge from ear is present.
■ symptoms are accompanied by a fever (over 101'F).

Drug Facts (continued)

SPL UNCLASSIFIED SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of the reach of children. If swallowed, contact a medical professional or Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Shake well before using.

Adults and children ages 2 years and over: TIit head sideways and apply 3·4 drops into involved ear (tip of applicator should not enter ear canal). Keep head tilted for at least 2 minutes to keep drops in ear. Repeat until relieved, up to 4 times daily.

Other information

OTHER SAFETY INFORMATION

■ Do not use If Imprinted "SEALED FOR YOUR PROTECTION" tamper-evident bottle cap band is broken or missing.
■ Store at room temperature.
■ Do nol refrigerate.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citric Acid, Glycerin, Purified Water, Sodium Benzoate.

SPL UNCLASSIFIED SECTION

*CLAIMS BASED ON TRADITIONAL

HOMEOPATHIC PRACTICE, NOT ACCEPTED

MEDICAL EVIDENCE. NOT FDA EVALUATED.

Questions or comments?

OTC - QUESTIONS SECTION

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915

SPL UNCLASSIFIED SECTION

Distributed by:

Wal-Mart Inc.,

Bentonville, AR 72716

Indications and Usage (Uses)

RECENT MAJOR CHANGES SECTION

Changed to "Temporarily relieves symptoms of earache after diagnosis by a physician, including: ■ minor fever ■ ear pain or

hroobing ■ irritability ■ occasional sleeplessness ■ common pain or itching of "swimmer's ear"

Dosage and Administration (Directions)

RECENT MAJOR CHANGES SECTION

Changed to: ■ Shake well before using. Adults and children ages 2 years and over: TIit head sideways and apply 3·4 drops into involved ear (tip of applicator should not enter ear canal). Keep head tilted for at least 2 minutes to keep drops in ear. Repeat until relieved, up to 4 times daily.

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-320-01

equate™

Compare
to Hyland's
Earache
Drops

active

ingredients

Homeopathic

Earache
Drops*

  • Relieves ear pain
  • Calms irritability
  • Soothes itching due to cold & flu, swimmer's ear

& allergies

0.33 FL OZ (10mL)

*CLAIMS BASED ON TRADITIONAL

HOMEOPATHIC PRACTICE, NOT ACCEPTED

MEDICAL EVIDENCE. NOT FDA EVALUATED.

cartoncarton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-320-012020-08-25C16284748780-19d75b9d1-0a41-f424-e053-dadaa90a57ceEquate Homeopathic Earache Drops
49035-320-012020-01-31C16284748780-19d75b9d1-0a41-f424-e053-dadaa90a57ceEquate Homeopathic Earache Drops

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4791
MATRICARIA RECUTITAACTIVE INGREDIENTG0R4UBI2ZZ1
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE INGREDIENT2E32821G6I1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SULFURACTIVE INGREDIENT70FD1KFU701
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4791
MATRICARIA RECUTITAACTIVE MOIETYG0R4UBI2ZZ1
OYSTER SHELL CALCIUM CARBONATE, CRUDEACTIVE MOIETY2E32821G6I1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
SULFURACTIVE MOIETY70FD1KFU701
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EU1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
49035-32049035-320-01

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 · Source PDF

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 4 · 198 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GLYCERINGLYCERINPDC6A3C0OXSYSTEM / IONTOPHORESIS168.1 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPCAPSULE / ORAL238 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOLUTION/ DROPS / TOPICAL0.01 %w/vExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXLOTION / TOPICAL3990 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXINJECTION, SOLUTION / SUBCUTANEOUS15 %w/vExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXTABLET, FILM COATED / ORAL1.55 mgExact identifier — unii candidate
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SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUFILM / BUCCAL1 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSOLUTION / AURICULAR (OTIC)63.64 %w/vExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXPASTE / ORAL3822 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPTABLET, EXTENDED RELEASE / ORAL45 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPCONCENTRATE / ORAL5.3 mg/1mlExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSUSPENSION/ DROPS / OPHTHALMIC2.5 %w/vExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPLIQUID / ORAL114 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPAEROSOL, FOAM / RECTAL7 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXCAPSULE, COATED / ORAL14.21 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXCREAM / VAGINAL60 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSOLUTION, CONCENTRATE / ORAL200 mg/1mlExact identifier — unii candidate
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SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUELIXIR / ORAL5.02 mg/5mlExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXGEL / OPHTHALMIC0.88 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSOLUTION, CONCENTRATE / INTRAVENOUSNAExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXCAPSULE, LIQUID FILLED / ORAL185 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSUSPENSION / OPHTHALMIC58 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INTRA-ARTICULARADJ PHExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPEMULSION / TOPICAL0.11 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INTRAMUSCULAR28 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION, SOLUTION / INTRAVENOUS396 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSYRUP / ORAL16734 mgExact identifier — unii candidate
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SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUTABLET, FILM COATED / ORAL1 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPLOTION / TOPICAL0.85 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPTABLET / SUBLINGUAL24 mgExact identifier — unii candidate
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SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUGRANULE / ORALNAExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPINJECTION / INFILTRATION0.02 %w/vExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXEMULSION / INTRAVENOUS2.2 %w/vExact identifier — unii candidate
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SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUPASTE / DENTAL0.08 %w/wExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSOLUTION / NASAL25 mg/1mlExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSWAB / TOPICAL0.05 %w/wExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPLIQUID / INTRAVENOUS0.2 %w/vExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXELIXIR / ORAL5621 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXGEL / TOPICAL500 mgExact identifier — unii candidate
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CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPDOUCHE / VAGINAL0.07 %w/wExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXLIQUID / TOPICAL2.5 %w/wExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXSPRAY, METERED / NASAL13 mgExact identifier — unii candidate
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GLYCERINGLYCERINPDC6A3C0OXINJECTION / SUBCUTANEOUS450 mgExact identifier — unii candidate
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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
087a1d09-38e2-d509-e063-6394a90ab8df1cf1d27a-5fd0-4304-9748-ef36f75099e52023-10-24WarningsExact identifier
spl set id: 1cf1d27a-5fd0-4304-9748-ef36f75099e5

Reported adverse events (FAERS/openFDA)#

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