FDA.reportPublic FDA data

Plumeria Rubra

Product NDC
37662-3345
11-digit product format
376623345
Labeler code
37662
Product ID
37662-3345_fe101e58-b959-14ec-e053-6294a90a6118
Type
HUMAN OTC DRUG
Nonproprietary name
Plumeria Rubra
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-06-13
Substance
PLUMERIA RUBRA WHOLE
Active strength
30 [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
Plumeria Rubra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PLUMERIA RUBRA WHOLE30 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii31FL06Y50D

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3345-1Plumeria Rubra80 in 1 VIAL, GLASSPELLET801
37662-3345-2Plumeria Rubra200 in 1 VIAL, GLASSPELLET2001
37662-3345-3Plumeria Rubra1200 in 1 BOTTLE, GLASSPELLET12001
37662-3345-4Plumeria Rubra4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3345PLUMERIA RUBRA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230615_fe101e58-b958-14ec-e053-6294a90a6118.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3345-13766233450180 PELLET in 1 VIAL, GLASS (37662-3345-1) 80 pellet2023-06-13NoNoHistorical
37662-3345-237662334502200 PELLET in 1 VIAL, GLASS (37662-3345-2) 200 pellet2023-06-13NoNoHistorical
37662-3345-3376623345031200 PELLET in 1 BOTTLE, GLASS (37662-3345-3) 1200 pellet2023-06-13NoNoHistorical
37662-3345-4376623345044000 PELLET in 1 BOTTLE, GLASS (37662-3345-4) 4000 pellet2023-06-13NoNoHistorical