FDA.reportPublic FDA data

Arnicare Leg Cramps

Product NDC
0220-9073
11-digit product format
002209073
Labeler code
0220
Product ID
0220-9073_1059edf1-c73b-9c04-e063-6294a90a1e1c
Type
HUMAN OTC DRUG
Nonproprietary name
ARNICA MONTANA, LACTIC ACID, L-, ZINC OXIDE
Dosage form
TABLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-06-15
Substance
ARNICA MONTANA; ZINC OXIDE; LACTIC ACID, L-
Active strength
9; 3; 3 [hp_C]/1; [hp_C]/1; [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Arnicare Leg Cramps
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARNICA MONTANA9 [hp_C]/1
ZINC OXIDE3 [hp_C]/1
LACTIC ACID, L-3 [hp_C]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O80TY208ZWInternal UNII lookup
SOI2LOH54ZInternal UNII lookup
F9S9FFU82NInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
6b658f98-d6e9-9ac9-e053-2991aa0ab3b0Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
cb89b86a-369e-4204-8910-ae797c503af3Product name120230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7Product name220180830
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
0220-9073-062023-02-06Arnicare Leg Cramps
0220-9073-902023-02-06Arnicare Leg Cramps
0220-9073-062023-01-30Arnicare Leg Cramps
0220-9073-902023-01-30Arnicare Leg Cramps

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9073-06Arnicare Leg Cramps11 in 1 TUBETABLET115
0220-9073-90Arnicare Leg Cramps11 in 1 TUBETABLET115
0220-9073-90Arnicare Leg Cramps33 in 1 PACKAGETABLET335

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9073ARNICARE LEG CRAMPS (ARNICA MONTANA, LACTIC ACID, L-, ZINC OXIDE) TABLET [BOIRON]5Current NDC, Legacy NDC, 3 package rows20240208_6b658f98-d6e9-9ac9-e053-2991aa0ab3b0.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
Arnicare Leg CrampsARNICA MONTANA, LACTIC ACID, L-, ZINC OXIDEBoiron6b658f98-d6e9-9ac9-e053-2991aa0ab3b02024-02-01Exact identifier
ndc (product): 0220-9073

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0220-9073-060022090730611 TABLET in 1 TUBE (0220-9073-06) 11 tablet2018-06-150000-00-00NoNoCurrent
0220-9073-900022090739033 TUBE in 1 PACKAGE (0220-9073-90) / 11 TABLET in 1 TUBE33 tube2018-06-150000-00-00NoNoCurrent