Titanium metallicum

Product NDC
0220-5031
11-digit product format
002205031
Labeler code
0220
Product ID
0220-5031_21b504bc-e12e-3a8e-e063-6294a90a7708
Type
HUMAN OTC DRUG
Nonproprietary name
TITANIUM
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-01-01
Substance
TITANIUM
Active strength
200 [kp_C]/200[kp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiD1JT611TNE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5031-41Titanium metallicum200 [kp_C] in 1 TUBEPELLET2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5031TITANIUM METALLICUM (TITANIUM) PELLET [BOIRON]1Current NDC, 1 package rows20240910_21b504bc-e12d-3a8e-e063-6294a90a7708.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0220-5031-4100220503141200 [kp_C] in 1 TUBE (0220-5031-41) 2024-01-01NoNoCurrent