NDC 55714-4844 – I-Sleep

Wormwood 20 [hp_X]/mL; Semecarpus Anacardium Juice 20 [hp_X]/mL; Silver Nitrate 20 [hp_X]/mL; Arsenic Trioxide 20 [hp_X]/mL; Atropa Belladonna 20 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC55714-4844

Product details

Brand name
I-Sleep
Generic name
Absinthium, Anacardium orientale, Arg. nit., Arsenicum alb., Belladonna, Bryonia, Calc. carb., Camphora, Chamomilla, Cimicifuga, Cinchona, Coffea cruda, Cypripedium, Gelsemium, Humulus, Hyoscyamus, Ignatia, Kali brom., Nux vom., Passiflora, Pulsatilla, Scutellaria lateriflora, Sepia, Thuja occ., Valeriana
Labeler
Newton Laboratories, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
February 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for I-Sleep →

Package NDC codes (1)

Package NDCDescriptionSince
55714-4844-130 mL in 1 BOTTLE, GLASS (55714-4844-1)Feb 1, 2021

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