NDC 50845-0109

PMS

Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cuprum Metallicum, Ignatia Amara, Kali Iodatum, Magnesia Phosphorica, Oophorinum (suis), Platinum Metallicum, Sepia, Thuja Occidentalis

PMS is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Liddell Laboratories, Inc.. The primary component is Apis Mellifera; Matricaria Recutita; Black Cohosh; Copper; Strychnos Ignatii Seed; Potassium Iodide; Magnesium Phosphate, Dibasic Trihydrate; Sus Scrofa Ovary; Platinum; Sepia Officinalis Juice; Thuja Occidentalis Leafy Twig.

• Product ID: 50845-0109_8d5f1c1c-ba48-45da-906c-496a2bf32693
• NDC: 50845-0109
• Product Type: Human Otc Drug
• Proprietary Name: PMS
• Generic Name: Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cuprum Metallicum, Ignatia Amara, Kali Iodatum, Magnesia Phosphorica, Oophorinum (suis), Platinum Metallicum, Sepia, Thuja Occidentalis
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2011-07-18
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Liddell Laboratories, Inc.
• Substance Name: APIS MELLIFERA; MATRICARIA RECUTITA; BLACK COHOSH; COPPER; STRYCHNOS IGNATII SEED; POTASSIUM IODIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SUS SCROFA OVARY; PLATINUM; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG
• Active Ingredient Strength: 200 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 50845-0109-2

1 BOTTLE, SPRAY in 1 CARTON (50845-0109-2) > 30 mL in 1 BOTTLE, SPRAY (50845-0109-1)

• Marketing Start Date: 2016-09-06
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50845-0109-1 [50845010901]

PMS SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-07-18

NDC 50845-0109-2 [50845010902]

PMS SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-09-06

NDC 50845-0109-3 [50845010903]

PMS SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-07-18
• Marketing End Date: 2016-08-11

Drug Details

Active Ingredients

Ingredient	Strength
APIS MELLIFERA	200 [hp_C]/mL

OpenFDA Data

• SPL SET ID: 575b4736-5bae-4f15-b55b-3e1fbbb613ff
• Manufacturer:
  • Liddell Laboratories, Inc.
• UNII:
  • S7YTV04R8O
  • 1C4QK22F9J
  • QDL83WN8C2
  • K73E24S6X9
  • 789U1901C5
  • 7S82P3R43Z
  • G0R4UBI2ZZ
  • 1NT28V9397
  • 1NM3M2487K
  • 49DFR088MY
  • HF539G9L3Q

NDC Crossover Matching brand name "PMS" or generic name "Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cuprum Metallicum, Ignatia Amara, Kali Iodatum, Magnesia Phosphorica, Oophorinum (suis), Platinum Metallicum, Sepia, Thuja Occidentalis"

NDC	Brand Name	Generic Name
43857-0314	PMS	Angelica Archangelica, Cimicifuga Racemosa, Fucus Vesiculosus, Hypothalamus Suis, Magnesium Gluconicum Dihydricum, Oophorinum (Suis) Pyridoxinum Hydrochloricum, Bovista, Cuprum Metallicum, Sepia, Zincum Metallicum, Lachesis Mutus
44911-0200	PMS	Belladonna, Kali Carbonicum, Lachesis Mutus, Magnesia Phosphorica, Natrum Muriaticum, Nux Vomica, Pulsatilla (Pratensis), Sepia
50845-0109	PMS	Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cuprum Metallicum, Ignatia Amara, Kali Iodatum, Magnesia Phosphorica, Oophorinum (Suis), Platinum Metallicum, Sepia, Thuja Occidentalis
54973-2957	PMS	VIBURNUM OPULUS BARK, CAULOPHYLLUM THALICTROIDES ROOT, ANAMIRTA COCCULUS SEED, and GELSEMIUM SEMPERVIRENS ROOT