FDA.reportPublic FDA data

Plumeria Rubra

Product NDC
37662-3347
11-digit product format
376623347
Labeler code
37662
Product ID
37662-3347_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
200 [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 WHOLE200 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii31FL06Y50D

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3347-1Plumeria Rubra200 in 1 VIAL, GLASSPELLET2001
37662-3347-2Plumeria Rubra500 in 1 VIAL, GLASSPELLET5001
37662-3347-3Plumeria Rubra3000 in 1 BOTTLE, GLASSPELLET30001
37662-3347-4Plumeria Rubra10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3347PLUMERIA 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
37662-3347-137662334701200 PELLET in 1 VIAL, GLASS (37662-3347-1) 200 pellet2023-06-13NoNoHistorical
37662-3347-237662334702500 PELLET in 1 VIAL, GLASS (37662-3347-2) 500 pellet2023-06-13NoNoHistorical
37662-3347-3376623347033000 PELLET in 1 BOTTLE, GLASS (37662-3347-3) 3000 pellet2023-06-13NoNoHistorical
37662-3347-43766233470410000 PELLET in 1 BOTTLE, GLASS (37662-3347-4) 10000 pellet2023-06-13NoNoHistorical