Pain Relief

Product NDC
70994-102
Requested package NDC
70994-102-04
11-digit product format
709940102
Labeler code
70994
Product ID
70994-102_4604cabb-ce1e-ae65-e063-6394a90a200e
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica, Menthol Crystals, Cinnamon, Peppermint, Ginger, Rosemary
Dosage form
SALVE
Route
TOPICAL
Labeler
Spry Life LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2016-03-31
Substance
ARNICA MONTANA FLOWER
Active strength
1 [hp_X]/17g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage70994-10270994-102-04UExcluded because listing certification expiredexcluded / ndc_excluded.ziped331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage70994-10270994-102-04UExcluded because listing certification expiredexcluded / ndc_excluded.zip0efc9e666f02…f202fb6c5f17…

Additional Listing Data#

Finished product
Yes
Brand name base
Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA FLOWER1 [hp_X]/17g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
OZ0E5Y15PZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
480dc24e-87d0-55db-e054-00144ff88e88Available on FDA.report

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70994-102PAIN RELIEF (ARNICA, MENTHOL CRYSTALS, CINNAMON, PEPPERMINT, GINGER, ROSEMARY) SALVE [SPRY LIFE LLC]6Current NDC, Legacy NDC, 6 package rows20250130_480dc24e-87d0-55db-e054-00144ff88e88.zip

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): 70994-102-04
ndc (product): 70994-102
ndc11 (package): 70994010204

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70994-102-047099401020417 g in 1 TUBE (70994-102-04) 17 g2019-02-050000-00-00NoNoCurrent