Acidum Oxalicum

Product NDC
37662-2518
11-digit product format
376622518
Labeler code
37662
Product ID
37662-2518_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
100 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0K2L2IJ59OOXALIC ACID DIHYDRATE6153-56-6OXALIC ACID DIHYDRATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2518-137662251801200 PELLET in 1 VIAL, GLASS (37662-2518-1) 200 pellet2023-01-25NoNoHistorical
37662-2518-237662251802500 PELLET in 1 VIAL, GLASS (37662-2518-2) 500 pellet2023-01-25NoNoHistorical
37662-2518-3376622518033000 PELLET in 1 BOTTLE, GLASS (37662-2518-3) 3000 pellet2023-01-25NoNoHistorical
37662-2518-43766225180410000 PELLET in 1 BOTTLE, GLASS (37662-2518-4) 10000 pellet2023-01-25NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Acidum Oxalicum - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-01-25HUMAN OTC DRUG LABEL1