FDA.reportPublic FDA data

BENZOICUM ACIDUM

Product NDC
0220-0820
11-digit product format
002200820
Labeler code
0220
Product ID
0220-0820_124e1676-96fe-1a52-e063-6294a90a901f
Type
HUMAN OTC DRUG
Nonproprietary name
BENZOIC ACID
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-01-01
Substance
BENZOIC ACID
Active strength
200 [kp_C]/200[kp_C]
Pharmacologic classes
Ammonium Ion Binding Activity [MoA], Nitrogen Binding Agent [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZOIC ACID200 [kp_C]/200[kp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8SKN0B0MIM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0820-41BENZOICUM ACIDUM200 [kp_C] in 1 TUBEPELLET2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0820BENZOICUM ACIDUM (BENZOIC ACID) PELLET [BOIRON]1Current NDC, 1 package rows20240228_124e1676-96fd-1a52-e063-6294a90a901f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0220-0820-4100220082041200 [kp_C] in 1 TUBE (0220-0820-41) 2024-01-01NoNoCurrent