Vanilla Planifolia

Product NDC
37662-3225
11-digit product format
376623225
Labeler code
37662
Product ID
37662-3225_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
100 [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
37662-3225-137662322501200 PELLET in 1 VIAL, GLASS (37662-3225-1) 200 pellet2023-05-23NoNoHistorical
37662-3225-237662322502500 PELLET in 1 VIAL, GLASS (37662-3225-2) 500 pellet2023-05-23NoNoHistorical
37662-3225-3376623225033000 PELLET in 1 BOTTLE, GLASS (37662-3225-3) 3000 pellet2023-05-23NoNoHistorical
37662-3225-43766232250410000 PELLET in 1 BOTTLE, GLASS (37662-3225-4) 10000 pellet2023-05-23NoNoHistorical

Related DailyMed Labels

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