FDA.reportPublic FDA data

Pain Away Solution

Manufacturer
Pure Source, LLC
Effective date
2017-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:54

Label at a glance#

ProductPain Away Solution
Active ingredientHYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, ACONITUM NAPELLUS, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, CLAVICEPS PURPUREA SCLEROTIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aconitum Napellus, 24X HPUS

Hypericum Peforatum, 24X HPUS

Lycopodium Clavatum, 24X HPUS

Phosphorus, 24X HPUS

Rhus Toxicodendron, 24X HPUS

Secale Cornuum, 24X HPUS

OTC - PURPOSE SECTION

Nerve Pain Relief

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away - (800-222-1222)

INDICATIONS & USAGE SECTION

Use

For the temporary relief of nerve pain

WARNINGS SECTION

Warnings

For external use only.

Do not use on wounds or damaged skin.

Stop use and ask doctor if

  • Symptoms persist for more than seven days.
  • If irritation occurs, discontinue use.

When using this product

  • Avoid contact with eyes.
  • Do not wrap treated area with bandage.

If pregnant or breast feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Spray small amount to cover the affected area.
  • Do not apply more than 4 times daily.
  • Avoid contact with eyes and mucus membranes.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Bergamot Oil, Cassia Leaf Oil, Eucalyptus Oil, Geranium Oil, Histamine Dihydrochloride, Lavender Oil, Safflower Oil, SD-Alcohol 38B, Tea Tree Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65121-887-012025-01-30C16284748780-12cef2736-a095-d83d-e063-dadaa90ab31f579b1f76-1297-684f-e053-2a91aa0a83d7
65121-887-022025-01-30C16284748780-12cef2736-a095-d83d-e063-dadaa90ab31f579b1f76-1297-684f-e053-2a91aa0a83d7
65121-887-032025-01-30C16284748780-12cef2736-a095-d83d-e063-dadaa90ab31f579b1f76-1297-684f-e053-2a91aa0a83d7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65121-887-01Pain Away Solution10 mL in 1 BOTTLE, GLASSSPRAY101
65121-887-02Pain Away Solution15 mL in 1 BOTTLE, GLASSSPRAY151
65121-887-03Pain Away Solution15 mL in 1 BOTTLE, SPRAYSPRAY151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65121-887PAIN AWAY SOLUTION (ACONITUM NEPELLUS HYPERICUM PEFORATUM LYCOPODIUM CLAVATUM PHOSPHORUS RHUS TOXICODENDRON SECALE CORNUTUM) SPRAY [PURE SOURCE, LLC]1Legacy NDC, 3 package rows20170826_579b1f76-1297-684f-e053-2a91aa0a83d7.zip

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
65121-88765121-887-01, 65121-887-02, 65121-887-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
EUCALYPTUS OIL2R04ONI662IACT
LAVENDER OILZBP1YXW0H8IACT
TEA TREE OILVIF565UC2GIACT
GERANIUM OIL, ALGERIAN TYPE5Q1I94P4WGIACT
ACONITUM NAPELLUSU0NQ8555JDACTIB
CHINESE CINNAMON LEAF OIL4U4V2F2E4YIACT
BERGAMOT OIL39W1PKE3JIIACT
PHOSPHORUS27YLU75U4WACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
CLAVICEPS PURPUREA SCLEROTIUM01G9XEA93NACTIB
SAFFLOWER OIL65UEH262ISIACT
HISTIDINE MONOHYDROCHLORIDE1D5Q932XM6IACT
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
58dea4a9-b8e0-9a1c-e063-6294a90ab9cf579b1f76-1297-684f-e053-2a91aa0a83d72026-08-12WarningsExact identifier
spl set id: 579b1f76-1297-684f-e053-2a91aa0a83d7

Reported adverse events (FAERS/openFDA)#

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