Hekla lava

Product NDC
0220-2393
11-digit product format
002202393
Labeler code
0220
Product ID
0220-2393_f9117281-c432-c08d-e053-6294a90af4eb
Type
HUMAN OTC DRUG
Nonproprietary name
HEKLA LAVA
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
HEKLA LAVA
Active strength
12 [hp_C]/12[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HEKLA LAVA12 [hp_C]/12[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiC21158IIRK

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2393-412023-04-11C16284748780-1f386c649-d288-0266-e053-dadaa90a7c1aHekla lava 12C
0220-2393-412023-01-30C16284748780-1f386c649-d288-0266-e053-dadaa90a7c1aHekla lava 12C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2393-41Hekla lava12 [hp_C] in 1 TUBEPELLET122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2393HEKLA LAVA (HEKLA LAVA ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230412_85b4f8db-bdc1-12d0-e053-2a91aa0a8c5b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2393-410022023934112 [hp_C] in 1 TUBE (0220-2393-41) 1983-03-030000-00-00NoNoCurrent