FDA.reportPublic FDA data

Aluminium Phosphoricum

Product NDC
37662-3581
11-digit product format
376623581
Labeler code
37662
Product ID
37662-3581_003ea3bc-9e9b-00ab-e063-6394a90aac24
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminium Phosphoricum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-07-11
Substance
ALUMINUM PHOSPHATE
Active strength
500 [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
Aluminium Phosphoricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALUMINUM PHOSPHATE500 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF92V3S521O

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3581-1Aluminium Phosphoricum200 in 1 VIAL, GLASSPELLET2001
37662-3581-2Aluminium Phosphoricum500 in 1 VIAL, GLASSPELLET5001
37662-3581-3Aluminium Phosphoricum3000 in 1 BOTTLE, GLASSPELLET30001
37662-3581-4Aluminium Phosphoricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3581ALUMINIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230712_003ea3bc-9e9a-00ab-e063-6394a90aac24.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3581-137662358101200 PELLET in 1 VIAL, GLASS (37662-3581-1) 200 pellet2023-07-11NoNoCurrent
37662-3581-237662358102500 PELLET in 1 VIAL, GLASS (37662-3581-2) 500 pellet2023-07-11NoNoCurrent
37662-3581-3376623581033000 PELLET in 1 BOTTLE, GLASS (37662-3581-3) 3000 pellet2023-07-11NoNoCurrent
37662-3581-43766235810410000 PELLET in 1 BOTTLE, GLASS (37662-3581-4) 10000 pellet2023-07-11NoNoCurrent