Vanilla Planifolia

Product NDC
37662-3223
11-digit product format
376623223
Labeler code
37662
Product ID
37662-3223_fc636b53-c038-2fef-e053-6394a90aaca6
Type
HUMAN OTC DRUG
Nonproprietary name
Vanilla Planifolia
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-05-23
Substance
VANILLA BEAN
Active strength
12 [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

Related Records

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3223-137662322301200 PELLET in 1 VIAL, GLASS (37662-3223-1) 200 pellet2023-05-23NoNoHistorical
37662-3223-2376623223021200 PELLET in 1 BOTTLE, GLASS (37662-3223-2) 1200 pellet2023-05-23NoNoHistorical
37662-3223-3376623223034000 PELLET in 1 BOTTLE, GLASS (37662-3223-3) 4000 pellet2023-05-23NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Vanilla Planifolia - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-05-23HUMAN OTC DRUG LABEL1