NDC 55926-0019

Morale Remedy No. 19

Anacardium Orientale, Aurum Metallicum, Calcarea Carbonica, Cimicifuga Racemosa, Hypericum Perforatum, Ignatia Amara, Kale Bromatum, Natrum Carbonicum, Natrum Sulphuricum, Phosphoricum Acidum, Phosphorus, Pulsatilla, Sepia, Tabacum

Morale Remedy No. 19 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Speer Laboratories, Llc. The primary component is Semecarpus Anacardium Juice; Gold; Oyster Shell Calcium Carbonate, Crude; Black Cohosh; Hypericum Perforatum; Strychnos Ignatii Seed; Potassium Bromide; Sodium Carbonate; Sodium Sulfate; Phosphoric Acid; Phosphorus; Pulsatilla Vulgaris; Sepia Officinalis Juice; Tobacco Leaf.

Product ID55926-0019_38b30db7-7ac2-49cf-b3c1-f99438c9ecf7
NDC55926-0019
Product TypeHuman Otc Drug
Proprietary NameMorale Remedy No. 19
Generic NameAnacardium Orientale, Aurum Metallicum, Calcarea Carbonica, Cimicifuga Racemosa, Hypericum Perforatum, Ignatia Amara, Kale Bromatum, Natrum Carbonicum, Natrum Sulphuricum, Phosphoricum Acidum, Phosphorus, Pulsatilla, Sepia, Tabacum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-07-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameSpeer Laboratories, LLC
Substance NameSEMECARPUS ANACARDIUM JUICE; GOLD; OYSTER SHELL CALCIUM CARBONATE, CRUDE; BLACK COHOSH; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; POTASSIUM BROMIDE; SODIUM CARBONATE; SODIUM SULFATE; PHOSPHORIC ACID; PHOSPHORUS; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; TOBACCO LEAF
Active Ingredient Strength10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 55926-0019-2

59 mL in 1 BOTTLE, SPRAY (55926-0019-2)
Marketing Start Date2013-07-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55926-0019-2 [55926001902]

Morale Remedy No. 19 LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-07-17
Inactivation Date2020-01-31

Drug Details


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