FDA.reportPublic FDA data

Eucalyptus Globulus

Product NDC
37662-0682
11-digit product format
376620682
Labeler code
37662
Product ID
37662-0682_e1fe022c-d1db-183a-e053-2995a90ae17f
Type
HUMAN OTC DRUG
Nonproprietary name
Eucalyptus Globulus
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-06-21
Substance
EUCALYPTUS GLOBULUS LEAF
Active strength
12 [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
Eucalyptus Globulus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EUCALYPTUS GLOBULUS LEAF12 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiS546YLW6E6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0682-1Eucalyptus Globulus200 in 1 VIAL, GLASSPELLET2001
37662-0682-2Eucalyptus Globulus1200 in 1 BOTTLE, GLASSPELLET12001
37662-0682-3Eucalyptus Globulus4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0682EUCALYPTUS GLOBULUS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220623_e1fe022c-d1da-183a-e053-2995a90ae17f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0682-137662068201200 PELLET in 1 VIAL, GLASS (37662-0682-1) 200 pellet2022-06-210000-00-00NoNoCurrent
37662-0682-2376620682021200 PELLET in 1 BOTTLE, GLASS (37662-0682-2) 1200 pellet2022-06-210000-00-00NoNoCurrent
37662-0682-3376620682034000 PELLET in 1 BOTTLE, GLASS (37662-0682-3) 4000 pellet2022-06-210000-00-00NoNoCurrent