Formalinum

Product NDC
0220-2135
11-digit product format
002202135
Labeler code
0220
Product ID
0220-2135_0a0ce624-1a01-85f4-e063-6294a90ac29a
Type
HUMAN OTC DRUG
Nonproprietary name
FORMALDEHYDE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
FORMALDEHYDE
Active strength
30 [hp_C]/30[hp_C]
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FORMALDEHYDE30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1HG84L3525

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2135-412023-11-13C16284748780-1f386c649-f167-0266-e053-dadaa90a7c1aFormalinum 30C
0220-2135-412023-01-30C16284748780-1f386c649-f167-0266-e053-dadaa90a7c1aFormalinum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2135-41Formalinum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2135FORMALINUM (FORMALDEHYDE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231114_87376732-58e9-40af-e053-2a91aa0a58f5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2135-410022021354130 [hp_C] in 1 TUBE (0220-2135-41) 1983-03-030000-00-00NoNoCurrent