FDA.reportPublic FDA data

Plumeria Rubra

Product NDC
37662-3350
11-digit product format
376623350
Labeler code
37662
Product ID
37662-3350_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
10 [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
Plumeria Rubra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PLUMERIA RUBRA WHOLE10 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii31FL06Y50D

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3350-1Plumeria Rubra200 in 1 VIAL, GLASSPELLET2001
37662-3350-2Plumeria Rubra500 in 1 VIAL, GLASSPELLET5001
37662-3350-3Plumeria Rubra3000 in 1 BOTTLE, GLASSPELLET30001
37662-3350-4Plumeria Rubra10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3350PLUMERIA 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
37662-3350-137662335001200 PELLET in 1 VIAL, GLASS (37662-3350-1) 200 pellet2023-06-13NoNoHistorical
37662-3350-237662335002500 PELLET in 1 VIAL, GLASS (37662-3350-2) 500 pellet2023-06-13NoNoHistorical
37662-3350-3376623350033000 PELLET in 1 BOTTLE, GLASS (37662-3350-3) 3000 pellet2023-06-13NoNoHistorical
37662-3350-43766233500410000 PELLET in 1 BOTTLE, GLASS (37662-3350-4) 10000 pellet2023-06-13NoNoHistorical