SP

Manufacturer
Chi Research, Inc. | Apotheca Company
Effective date
2024-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:26:42

Label at a glance#

ProductSP
Active ingredientPIPER ADUNCUM LEAF, SMILAX ORNATA WHOLE, THUJA OCCIDENTALIS LEAFY TWIG, UNCARIA TOMENTOSA ROOT, PHYLLANTHUS NIRURI WHOLE, REYNOUTRIA JAPONICA WHOLE
Label structure9 sections

Dosage and administration

Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Matico 32X, Sarsaparilla (Smilax Regelii) 32X, Thuja Occidentalis 32X, Uncaria Tomentosa 32X, Phyllanthus Niruri 32C, Polygonum Cuspidatum 32C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms of musculoskeletal discomfort.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use. Consult a physician for use in children under 12 years of age.

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

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms of musculoskeletal discomfort.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by

Chi Research, Inc.

207 6th Street South

Walker, MN 56484

218-547-1775

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CHI

RESEARCH

SP

Homeopathic Remedy

4 fl. oz. (120 ml)

SPSP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52654-0006-12024-04-22C16284748780-1d6a99b39-3915-a426-e053-dadaa90af4c2DRUG FACTS:
52654-0006-12022-01-28C16284748780-1d6a99b39-3915-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52654-0006-1SP120 mL in 1 BOTTLE, DROPPERLIQUID1202

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52654-0006SP (MATICO, SARSAPARILLA (SMILAX REGELII), THUJA OCCIDENTALIS, UNCARIA TOMENTOSA, PHYLLANTHUS NIRURI, POLYGONUM CUSPIDATUM) LIQUID [CHI RESEARCH, INC.]2Current NDC, Legacy NDC, 1 package rows20240423_12b8ef27-179e-4920-bcd3-856daada1a6a.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52654-000652654-0006-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
SPMATICO, SARSAPARILLA (SMILAX REGELII), THUJA OCCIDENTALIS, UNCARIA TOMENTOSA, PHYLLANTHUS NIRURI, POLYGONUM CUSPIDATUMChi Research, Inc.12b8ef27-179e-4920-bcd3-856daada1a6a2024-04-22WarningsExact identifier
ndc (package): 52654-0006-1
ndc (product): 52654-0006
ndc11 (package): 52654000601
spl id: 2bcbcb9c-712d-417a-9163-b6a4520f1ab1
spl set id: 12b8ef27-179e-4920-bcd3-856daada1a6a

Reported adverse events (FAERS/openFDA)#

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