NDC 50845-0162

POSTPARTUM BLUES

Aconitum Napellus, Ambra Grisea, Hypericum Perforatum, Ignatia Amara, Nux Vomica, Spigelia Anthelmia

POSTPARTUM BLUES is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Liddell Laboratories, Inc.. The primary component is Aconitum Napellus; Ambergris; Hypericum Perforatum; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Spigelia Anthelmia.

Product ID50845-0162_39d2f54b-2ec3-4bf5-8374-10523b32200e
NDC50845-0162
Product TypeHuman Otc Drug
Proprietary NamePOSTPARTUM BLUES
Generic NameAconitum Napellus, Ambra Grisea, Hypericum Perforatum, Ignatia Amara, Nux Vomica, Spigelia Anthelmia
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2015-01-13
Marketing End Date2024-02-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameLiddell Laboratories, Inc.
Substance NameACONITUM NAPELLUS; AMBERGRIS; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; SPIGELIA ANTHELMIA
Active Ingredient Strength30 [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
NDC Exclude FlagN

Packaging

NDC 50845-0162-2

1 BOTTLE, SPRAY in 1 CARTON (50845-0162-2) > 30 mL in 1 BOTTLE, SPRAY (50845-0162-1)
Marketing Start Date2015-01-13
Marketing End Date2024-02-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50845-0162-2 [50845016202]

POSTPARTUM BLUES SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-13
Inactivation Date2020-01-31

NDC 50845-0162-1 [50845016201]

POSTPARTUM BLUES SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-01-13

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS30 [hp_C]/mL

OpenFDA Data

SPL SET ID:8e92952f-e72c-43a4-a0c3-47fef6f1ac86
Manufacturer
UNII

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.