FDA.reportPublic FDA data

Cinnabaris

Product NDC
37662-0322
11-digit product format
376620322
Labeler code
37662
Product ID
37662-0322_e093713d-a0f6-cc29-e053-2995a90aa2e3
Type
HUMAN OTC DRUG
Nonproprietary name
Cinnabaris
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-03
Substance
MERCURIC SULFIDE
Active strength
6 [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
Cinnabaris
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MERCURIC SULFIDE6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZI0T668SF1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0322-1Cinnabaris200 in 1 VIAL, GLASSPELLET2001
37662-0322-2Cinnabaris1200 in 1 BOTTLE, GLASSPELLET12001
37662-0322-3Cinnabaris4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0322CINNABARIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220604_e093713d-a0f5-cc29-e053-2995a90aa2e3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0322-137662032201200 PELLET in 1 VIAL, GLASS (37662-0322-1) 200 pellet2022-06-030000-00-00NoNoCurrent
37662-0322-2376620322021200 PELLET in 1 BOTTLE, GLASS (37662-0322-2) 1200 pellet2022-06-030000-00-00NoNoCurrent
37662-0322-3376620322034000 PELLET in 1 BOTTLE, GLASS (37662-0322-3) 4000 pellet2022-06-030000-00-00NoNoCurrent