NDC 49726-016

Premensa PMS Symptom Relief

Apis Mellifica, Chamomilla, Cimicifuga Racemosa, Cyclamen Europaeum, Helonias Dioca, Ignatia Amara, Lac Caninum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Platinum Metallicum, Sepia

Premensa PMS Symptom Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Apis Mellifera; Chamomile; Black Cohosh; Cyclamen Purpurascens Tuber; Chamaelirium Luteum Root; Strychnos Ignatii Seed; Canis Lupus Familiaris Milk; Lycopodium Clavatum Spore; Sodium Chloride; Strychnos Nux-vomica Seed; Platinum; Sepia Officinalis Juice.

Product ID49726-016_7df0b4ca-2f66-e8e5-e053-2991aa0af9ee
NDC49726-016
Product TypeHuman Otc Drug
Proprietary NamePremensa PMS Symptom Relief
Generic NameApis Mellifica, Chamomilla, Cimicifuga Racemosa, Cyclamen Europaeum, Helonias Dioca, Ignatia Amara, Lac Caninum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Platinum Metallicum, Sepia
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-02-21
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHello Life, Inc.
Substance NameAPIS MELLIFERA; CHAMOMILE; BLACK COHOSH; CYCLAMEN PURPURASCENS TUBER; CHAMAELIRIUM LUTEUM ROOT; STRYCHNOS IGNATII SEED; CANIS LUPUS FAMILIARIS MILK; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PLATINUM; SEPIA OFFICINALIS JUICE
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
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49726-016-02

1 BOTTLE, DROPPER in 1 CARTON (49726-016-02) > 59 mL in 1 BOTTLE, DROPPER
Marketing Start Date2011-02-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49726-016-02 [49726001602]

Premensa PMS Symptom Relief LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-02-21
Inactivation Date2020-01-31

Drug Details


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