FDA.reportPublic FDA data

Back Pain

Product NDC
51393-4015
11-digit product format
513934015
Labeler code
51393
Product ID
51393-4015_4b48f15c-9c9b-e00b-e063-6294a90aa455
Type
HUMAN OTC DRUG
Nonproprietary name
Arnica Montana, HORSE CHESTNUT, Hypericum Perforatum, RUTA GRAVEOLENS WHOLE, and SODIUM CHLORIDE
Dosage form
SOLUTION/ DROPS
Route
TOPICAL
Labeler
Forces of Nature
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-11-01
Substance
ARNICA MONTANA WHOLE; HORSE CHESTNUT; HYPERICUM PERFORATUM WHOLE; RUTA GRAVEOLENS WHOLE; SODIUM CHLORIDE
Active strength
30; 6; 12; 30; 30 [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage51393-401551393-4015-1DDiscontinued by firm2026-08-07

Additional Listing Data#

Finished product
Yes
Brand name base
Back Pain
Brand name suffix
Pain Management
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA WHOLE30 [hp_C]/100mL
HORSE CHESTNUT6 [hp_C]/100mL
HYPERICUM PERFORATUM WHOLE12 [hp_C]/100mL
RUTA GRAVEOLENS WHOLE30 [hp_C]/100mL
SODIUM CHLORIDE30 [hp_C]/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 5 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup
3C18L6RJAZInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
181JI0338PInternal UNII lookup
451W47IQ8XInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
bf089347-f334-4d6d-ab58-cf7f0b16810fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51393-4015-12026-01-29C16284748780-149896155-bee6-586f-e063-e6dba90add90Back Pain Pain Management
51393-4015-42026-01-29C16284748780-149896155-bee6-586f-e063-e6dba90add90Back Pain Pain Management

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-4015-1Back PainPain Management11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS114
51393-4015-1Back PainPain Management1 in 1 CARTONSOLUTION/ DROPS14
51393-4015-4Back PainPain Management1 in 1 CARTONSOLUTION/ DROPS14
51393-4015-4Back PainPain Management4 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS44

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51393-4015BACK PAIN PAIN MANAGEMENT (ARNICA MONTANA, HORSE CHESTNUT, HYPERICUM PERFORATUM, RUTA GRAVEOLENS WHOLE, AND SODIUM CHLORIDE) SOLUTION/ DROPS [FORCES OF NATURE]3Current NDC, Legacy NDC, 4 package rows20221027_bf089347-f334-4d6d-ab58-cf7f0b16810f.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
Back Pain Pain ManagementARNICA MONTANA, HORSE CHESTNUT, HYPERICUM PERFORATUM, RUTA GRAVEOLENS WHOLE, AND SODIUM CHLORIDEForces of Naturebf089347-f334-4d6d-ab58-cf7f0b16810f2026-02-20WarningsExact identifier
ndc (product): 51393-4015

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
51393-4015-1513934015011 BOTTLE, DISPENSING in 1 CARTON (51393-4015-1) > 11 mL in 1 BOTTLE, DISPENSING2019-11-010000-00-00NoNoCurrent
51393-4015-4513934015041 BOTTLE, DISPENSING in 1 CARTON (51393-4015-4) / 4 mL in 1 BOTTLE, DISPENSING2019-11-010000-00-00NoNoCurrent