FDA.reportPublic FDA data

Vanilla Planifolia

Product NDC
37662-3287
11-digit product format
376623287
Labeler code
37662
Product ID
37662-3287_fd0c1104-0622-e706-e053-6294a90aec82
Type
HUMAN OTC DRUG
Nonproprietary name
Vanilla Planifolia
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-06-02
Substance
VANILLA
Active strength
6 [hp_C]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Vanilla Planifolia
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
VANILLA6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiQ74T35078H

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-3287-1Vanilla Planifolia200 in 1 VIAL, GLASSPELLET2001
37662-3287-2Vanilla Planifolia1200 in 1 BOTTLE, GLASSPELLET12001
37662-3287-3Vanilla Planifolia4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-3287VANILLA PLANIFOLIA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 3 package rows20230603_fd0c162a-6c2d-4b37-e053-6294a90a6d8f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3287-137662328701200 PELLET in 1 VIAL, GLASS (37662-3287-1) 200 pellet2023-06-02NoNoHistorical
37662-3287-2376623287021200 PELLET in 1 BOTTLE, GLASS (37662-3287-2) 1200 pellet2023-06-02NoNoHistorical
37662-3287-3376623287034000 PELLET in 1 BOTTLE, GLASS (37662-3287-3) 4000 pellet2023-06-02NoNoHistorical