FDA.reportPublic FDA data

Aluminium Phosphoricum

Product NDC
37662-3583
11-digit product format
376623583
Labeler code
37662
Product ID
37662-3583_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
10 [hp_M]/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 PHOSPHATE10 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF92V3S521O

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3583-1Aluminium Phosphoricum200 in 1 VIAL, GLASSPELLET2001
37662-3583-2Aluminium Phosphoricum500 in 1 VIAL, GLASSPELLET5001
37662-3583-3Aluminium Phosphoricum3000 in 1 BOTTLE, GLASSPELLET30001
37662-3583-4Aluminium Phosphoricum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3583ALUMINIUM 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
37662-3583-137662358301200 PELLET in 1 VIAL, GLASS (37662-3583-1) 200 pellet2023-07-11NoNoCurrent
37662-3583-237662358302500 PELLET in 1 VIAL, GLASS (37662-3583-2) 500 pellet2023-07-11NoNoCurrent
37662-3583-3376623583033000 PELLET in 1 BOTTLE, GLASS (37662-3583-3) 3000 pellet2023-07-11NoNoCurrent
37662-3583-43766235830410000 PELLET in 1 BOTTLE, GLASS (37662-3583-4) 10000 pellet2023-07-11NoNoCurrent