EARACHE- aconitum napellus, anthracinum, arnica montana, baptisia tinctoria, capsicum annuum, chamomilla, chenopodium anthelminticum, euphorbium officinarum, lachesis mutus, magnesia phosphorica, spray
Liddell Laboratories, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Earache

ACTIVE INGREDIENTS: Aconitum napellus 200C, Anthracinum 200C, Arnica montana 200C, Bapisia tinctoria 3X, Capsicum annuum 6X, Chamomilla 3X, Chenopodium anthelminticum 4X, Euphorbium officinarum 4X, Lachesis mutus 200C, Magnesia phosphorica 8X, Mercurius corrosivus 200C, Plantago major 3X, Pulsatilla 30X, Verbascum thapsus 3X.

INDICATIONS: Temporarily relieves symptoms associated with earache: pain, inflammation, discharge, burning sensation.

WARNINGS: If symptoms persist, consult a doctor.

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.

DIRECTIONS: Adults and children over 12: Place 15 drops under the tongue up to 6 times per day until symptoms are relieved.

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

INACTIVE INGREDIENTS: Organic alcohol 20% v/v, Purified water.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or call a Poison Control Center right away.

INDICATIONS: Temporarily relieves symptoms associated with earache: pain, inflammation, discharge, burning sensation.

LIDDELL LABORATORIES

WOODBINE, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

ORAL SPRAYS

LIDDELL LABORATORIES

Ear

Earache

HOMEOPATHIC

1.0 FL. OZ. (30 ml)

Earache

EARACHE
aconitum napellus, anthracinum, arnica montana, baptisia tinctoria, capsicum annuum, chamomilla, chenopodium anthelminticum, euphorbium officinarum, lachesis mutus, magnesia phosphorica, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50845-0119
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	200 [hp_C] in 1 mL
BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (BACILLUS ANTHRACIS IMMUNOSERUM RABBIT - UNII:41LZ22DD4N)	BACILLUS ANTHRACIS IMMUNOSERUM RABBIT	200 [hp_C] in 1 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	200 [hp_C] in 1 mL
BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU)	BAPTISIA TINCTORIA ROOT	3 [hp_X] in 1 mL
CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG)	CAPSICUM	6 [hp_X] in 1 mL
CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X)	CHAMOMILE	3 [hp_X] in 1 mL
CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (CHENOPODIUM AMBROSIOIDES - UNII:4H5RSU087I)	CHENOPODIUM AMBROSIOIDES	4 [hp_X] in 1 mL
EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K)	EUPHORBIA RESINIFERA RESIN	4 [hp_X] in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	200 [hp_C] in 1 mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE	8 [hp_X] in 1 mL
MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42)	MERCURIC CHLORIDE	200 [hp_C] in 1 mL
PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U)	PLANTAGO MAJOR	3 [hp_X] in 1 mL
ANEMONE PULSATILLA (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	ANEMONE PULSATILLA	30 [hp_X] in 1 mL
VERBASCUM THAPSUS (UNII: C9TD27U172) (VERBASCUM THAPSUS - UNII:C9TD27U172)	VERBASCUM THAPSUS	3 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50845-0119-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/25/2011	03/24/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		01/25/2011	03/24/2019

Labeler - Liddell Laboratories, Inc. (832264241)

Name	Address	ID/FEI	Business Operations
Establishment
Liddell Laboratories, Inc.		832264241	manufacture(50845-0119)

Revised: 1/2019

Document Id: 45dccfc2-1790-436c-9272-9f44518ba87f

Set id: 36b36980-99f9-44fc-9c22-a2e1df4c9517

Version: 2

Effective Time: 20190115

Liddell Laboratories, Inc.