FDA.reportPublic FDA data

Unique Pain Reduction Arthritis

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2021-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:22:05

Label at a glance#

ProductUnique Pain Reduction Arthritis
Active ingredientACONITUM NAPELLUS, APIS MELLIFERA, BENZOIC ACID, SUS SCROFA CARTILAGE, COLCHICUM AUTUMNALE BULB, EUPATORIUM PERFOLIATUM FLOWERING TOP, GUAIACUM OFFICINALE RESIN, HYPERICUM PERFORATUM, LEDUM PALUSTRE TWIG, MERCURIC CHLORIDE, TOXICODENDRON PUBESCENS LEAF, THUJA OCCIDENTALIS LEAFY TWIG
Label structure9 sections

Dosage and administration

Adults and children over 12: Spray twice under the tongue 3 times per day. Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aconitum Napellus 200C, Apis Mellifica 200C, Benzoicum Acidum 3X, Cartilago Suis 6X, Colchicum Autumnale 200C, Eupatorium Perfoliatum 200C, Guaiacum 3X, Hypericum Perforatum 200C, Ledum Palustre 6X, Mercurius Corrosivus 200C, Rhus Tox 200C, Thuja Occidentalis 200C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve minor aches and pains.**

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

WARNINGS:

WARNINGS SECTION

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.

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: Spray twice under the tongue 3 times per day.

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

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve minor aches and pains.**

**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

Unique Pain

Reduction +

Arthritis

HOMEOPATHIC

1.0 FL OZ (30 ml)

Unique Pain Reduction + ArthritisUnique Pain Reduction + Arthritis

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0184-12021-12-20C16284748780-19d75b9d1-03a2-f424-e053-dadaa90a57ceDrug Facts:
50845-0184-12020-01-31C16284748780-19d75b9d1-03a2-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-018450845-0184-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
APIS MELLIFERA7S82P3R43ZACTIB
BENZOIC ACID8SKN0B0MIMACTIB
SUS SCROFA CARTILAGE73ECW5WG2FACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
GUAIACUM OFFICINALE RESINN0K2Z502R6ACTIB
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
MERCURIC CHLORIDE53GH7MZT1RACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
d3e91485-41bc-46f1-93e5-e375ccb77b98d2cf78d8-afa6-4736-88e1-40371de0d1c72021-12-20WarningsExact identifier
spl id: d3e91485-41bc-46f1-93e5-e375ccb77b98
spl set id: d2cf78d8-afa6-4736-88e1-40371de0d1c7

Reported adverse events (FAERS/openFDA)#

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