Alumina silicata

Product NDC
0220-0209
11-digit product format
002200209
Labeler code
0220
Product ID
0220-0209_16dd93cc-6b7d-5b19-e063-6394a90aa244
Type
HUMAN OTC DRUG
Nonproprietary name
KAOLIN
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
KAOLIN
Active strength
30 [hp_C]/30[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
Alumina silicata
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
KAOLIN30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii24H4NWX5CO

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0209-412023-10-17C16284748780-1f386c649-b3bb-0266-e053-dadaa90a7c1aAlumina silicata 30C
0220-0209-412023-01-30C16284748780-1f386c649-b3bb-0266-e053-dadaa90a7c1aAlumina silicata 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0209-41Alumina silicata30 [hp_C] in 1 TUBEPELLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0209ALUMINA SILICATA (KAOLIN) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20240426_83ea8d43-c4d9-c9e2-e053-2991aa0af080.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0209-410022002094130 [hp_C] in 1 TUBE (0220-0209-41) 1983-03-030000-00-00NoNoCurrent