FDA.reportPublic FDA data

Aluminum Muriaticum

Product NDC
37662-2708
11-digit product format
376622708
Labeler code
37662
Product ID
37662-2708_f56a0700-4416-2dbb-e053-2995a90a3a03
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Muriaticum
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-02-23
Substance
ALUMINUM CHLORIDE ANHYDROUS
Active strength
1 [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
Aluminum Muriaticum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALUMINUM CHLORIDE ANHYDROUS1 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiLIF1N9568Y

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2708-1Aluminum Muriaticum200 in 1 VIAL, GLASSPELLET2001
37662-2708-2Aluminum Muriaticum500 in 1 VIAL, GLASSPELLET5001
37662-2708-3Aluminum Muriaticum3000 in 1 BOTTLE, GLASSPELLET30001
37662-2708-4Aluminum Muriaticum10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2708ALUMINUM MURIATICUM PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230225_f56a0700-4415-2dbb-e053-2995a90a3a03.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2708-137662270801200 PELLET in 1 VIAL, GLASS (37662-2708-1) 200 pellet2023-02-23NoNoCurrent
37662-2708-237662270802500 PELLET in 1 VIAL, GLASS (37662-2708-2) 500 pellet2023-02-23NoNoCurrent
37662-2708-3376622708033000 PELLET in 1 BOTTLE, GLASS (37662-2708-3) 3000 pellet2023-02-23NoNoCurrent
37662-2708-43766227080410000 PELLET in 1 BOTTLE, GLASS (37662-2708-4) 10000 pellet2023-02-23NoNoCurrent