Pain

Product NDC
50845-0265
Requested package NDC
50845-0265-1
11-digit product format
508450265
Labeler code
50845
Product ID
50845-0265_98ae5431-1b62-4394-a9b9-cb8c45f674f2
Type
HUMAN OTC DRUG
Nonproprietary name
Aconitum Napellus, Arnica Montana, Bellis Perennis, Bryonia (Alba), Cartilago Suis, Causticum, Chamomilla, Coffea Cruda, Euphorbium Officinarum, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Passiflora Incarnata, Pyrogenium, Ranunculus Bulbosus, Symphytum Officinale
Dosage form
SPRAY
Route
ORAL
Labeler
Liddell Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-03-26
Substance
ACONITUM NAPELLUS WHOLE; ARABICA COFFEE BEAN; ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CAUSTICUM; COMFREY ROOT; EUPHORBIA RESINIFERA RESIN; HYPERICUM PERFORATUM WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA CHAMOMILLA WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE; RANCID BEEF; RANUNCULUS BULBOSUS WHOLE; SUS SCROFA CARTILAGE
Active strength
200; 200; 3; 3; 12; 200; 6; 6; 200; 12; 3; 1; 3; 200; 6; 6 [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 · 3 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
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage50845-026550845-0265-1IInactivated by FDAexcluded / ndc_excluded.zipfb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage50845-026550845-0265-1IInactivated by FDAexcluded / ndc_excluded.zip86f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage50845-026550845-0265-1IInactivated by FDAexcluded / ndc_excluded.zipbd6a592717d7…303034d00443…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS WHOLE200 [hp_C]/mL
ARNICA MONTANA WHOLE200 [hp_C]/mL
BELLIS PERENNIS WHOLE3 [hp_X]/mL
BRYONIA ALBA ROOT3 [hp_X]/mL
SUS SCROFA CARTILAGE12 [hp_X]/mL
CAUSTICUM200 [hp_C]/mL
MATRICARIA CHAMOMILLA WHOLE6 [hp_X]/mL
ARABICA COFFEE BEAN6 [hp_X]/mL
EUPHORBIA RESINIFERA RESIN200 [hp_C]/mL
PSEUDOGNAPHALIUM OBTUSIFOLIUM WHOLE12 [hp_X]/mL
HYPERICUM PERFORATUM WHOLE3 [hp_X]/mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE1 [hp_X]/mL
PASSIFLORA INCARNATA FLOWERING TOP3 [hp_X]/mL
RANCID BEEF200 [hp_C]/mL
RANUNCULUS BULBOSUS WHOLE6 [hp_X]/mL
COMFREY ROOT6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 16 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
U0NQ8555JDInternal UNII lookup
O80TY208ZWInternal UNII lookup
2HU33I03UYInternal UNII lookup
T7J046YI2BInternal UNII lookup
73ECW5WG2FInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
G0R4UBI2ZZInternal UNII lookup
3SW678MX72Internal UNII lookup
1TI1O9028KInternal UNII lookup
36XQ854NWWInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
HF539G9L3QInternal UNII lookup
CLF5YFS11OInternal UNII lookup
29SUH5R3HUInternal UNII lookup
AEQ8NXJ0MBInternal UNII lookup
M9VVZ08EKQInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
b591e679-b481-47f1-8d4e-3f3040e9a42aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0265-12023-12-19C16284748780-1d6a99b39-8848-a426-e053-dadaa90af4c2DRUG FACTS:
50845-0265-12022-01-28C16284748780-1d6a99b39-8848-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50845-0265-1Pain30 mL in 1 BOTTLE, SPRAYSPRAY302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50845-0265PAIN (ACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALE) SPRAY [LIDDELL LABORATORIES, INC.]2Current NDC, Legacy NDC, 1 package rows20231220_b591e679-b481-47f1-8d4e-3f3040e9a42a.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
PainACONITUM NAPELLUS, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA (ALBA), CARTILAGO SUIS, CAUSTICUM, CHAMOMILLA, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, PYROGENIUM, RANUNCULUS BULBOSUS, SYMPHYTUM OFFICINALELiddell Laboratories, Inc.b591e679-b481-47f1-8d4e-3f3040e9a42a2023-12-19WarningsExact identifier
ndc (package): 50845-0265-1
ndc (product): 50845-0265
ndc11 (package): 50845026501

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50845-0265-15084502650130 mL in 1 BOTTLE, SPRAY (50845-0265-1) 30 ml2020-03-260000-00-00NoNoCurrent