FDA.reportPublic FDA data

Pain Relief

Manufacturer
Spry Life LLC
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:35:50

Label at a glance#

ProductPain Relief
Active ingredientARNICA MONTANA FLOWER
Label structure9 sections

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

External Analgesic

OTC Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Organic Arnica montana (Arnica) 1X (HPUS)

Indications & Usage

INDICATIONS & USAGE SECTION

■ temporarily reief of minor aches and pains of muscles and joints associated with ■ arthritis ■ bruises ■ sprains ■ scrapes ■ strains ■ simple backache ■ sore muscles

Warnings

WARNINGS SECTION

Warnings

For external use only.

■ Avoid contact with eyes.
■ Do not use on ■ on deep wounds ■ animal bites ■ serious burns
■ Stop use and ask a doctor if ■ condition worsens ■ symptoms last more than 7 days or clear up and occur again within a few days

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children.

Storage and Handling

STORAGE AND HANDLING SECTION

Store at room temperature.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected area
not more than 3 to 4 times daily. Children under 2 years of age: consult a physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Organic Olea Europaea (Olive) Fruit Oil, Organic Cera Alba (Beeswax), Organic Helianthus Annuus (Sunflower) Seed Oil, Organic Menthol, Mentha Piperita (Peppermint) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Zingiber Officinale (Ginger) Root Oil, Cinnamomum Zeylanicum Bark (Cinnamon) Oil.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pain Relief Principal Panel-BackPain Relief Principal Panel-Back

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70994-102-01Pain Relief19.8 g in 1 CANSALVE19.87
70994-102-02Pain Relief51.7 g in 1 CANSALVE51.77
70994-102-04Pain Relief17 g in 1 TUBESALVE177
70994-102-08Pain Relief113.4 g in 1 JARSALVE113.47
70994-102-09Pain Relief1 in 1 BOXSALVE17
70994-102-10Pain Relief1 in 1 BOXSALVE17

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70994-10270994-102-04, 70994-102-01, 70994-102-09, 70994-102-02, 70994-102-10, 70994-102-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
OLIVE OIL6UYK2W1W1EIACT
YELLOW WAX2ZA36H0S2VIACT
SUNFLOWER OIL3W1JG795YIIACT
MENTHOLL7T10EIP3AIACT
ROSEMARY OIL8LGU7VM393IACT
CINNAMON OILE5GY4I6YCZIACT
GINGER OILSAS9Z1SVUKIACT
MENTHA PIPERITA79M2M2UDA9IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZACTIB

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
Pain ReliefARNICA, MENTHOL CRYSTALS, CINNAMON, PEPPERMINT, GINGER, ROSEMARYSpry Life LLC480dc24e-87d0-55db-e054-00144ff88e882025-12-15WarningsExact identifier
ndc (package): 70994-102-01
ndc (package): 70994-102-04
ndc (package): 70994-102-08
ndc (package): 70994-102-10
ndc (package): 70994-102-02
ndc (package): 70994-102-09
ndc (product): 70994-102
ndc11 (package): 70994010209
ndc11 (package): 70994010210
ndc11 (package): 70994010208
ndc11 (package): 70994010204
ndc11 (package): 70994010201
ndc11 (package): 70994010202
spl id: 4604cabb-ce1e-ae65-e063-6394a90a200e
spl set id: 480dc24e-87d0-55db-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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