FDA.reportPublic FDA data

Acidum Oxalicum

Product NDC
37662-2517
11-digit product format
376622517
Labeler code
37662
Product ID
37662-2517_f323df0f-a3ff-6230-e053-2995a90a6252
Type
HUMAN OTC DRUG
Nonproprietary name
Acidum Oxalicum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-25
Substance
OXALIC ACID DIHYDRATE
Active strength
30 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OXALIC ACID DIHYDRATE30 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0K2L2IJ59O

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2517-1Acidum Oxalicum80 in 1 VIAL, GLASSPELLET801
37662-2517-2Acidum Oxalicum200 in 1 VIAL, GLASSPELLET2001
37662-2517-3Acidum Oxalicum1200 in 1 BOTTLE, GLASSPELLET12001
37662-2517-4Acidum Oxalicum4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2517ACIDUM OXALICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230127_f323df0f-a3fe-6230-e053-2995a90a6252.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2517-13766225170180 PELLET in 1 VIAL, GLASS (37662-2517-1) 80 pellet2023-01-25NoNoCurrent
37662-2517-237662251702200 PELLET in 1 VIAL, GLASS (37662-2517-2) 200 pellet2023-01-25NoNoCurrent
37662-2517-3376622517031200 PELLET in 1 BOTTLE, GLASS (37662-2517-3) 1200 pellet2023-01-25NoNoCurrent
37662-2517-4376622517044000 PELLET in 1 BOTTLE, GLASS (37662-2517-4) 4000 pellet2023-01-25NoNoCurrent