NDC 43857-0041

ANX HP

Arsenicum Album, Calcarea Carbonica, Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum

ANX HP is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Arsenic Trioxide; Oyster Shell Calcium Carbonate, Crude; Strychnos Ignatii Seed; Potassium Carbonate; Lachesis Muta Venom; Sodium Chloride; Phosphorus; Pulsatilla Vulgaris.

Product ID43857-0041_8307ff37-f16d-4890-9a51-95b4dd25af16
NDC43857-0041
Product TypeHuman Otc Drug
Proprietary NameANX HP
Generic NameArsenicum Album, Calcarea Carbonica, Ignatia Amara, Kali Carbonicum, Lachesis Mutus, Natrum Muriaticum
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-01-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBioActive Nutritional, Inc.
Substance NameARSENIC TRIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; STRYCHNOS IGNATII SEED; POTASSIUM CARBONATE; LACHESIS MUTA VENOM; SODIUM CHLORIDE; PHOSPHORUS; PULSATILLA VULGARIS
Active Ingredient Strength30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43857-0041-1

30 mL in 1 BOTTLE, DROPPER (43857-0041-1)
Marketing Start Date2017-06-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43857-0041-1 [43857004101]

ANX HP LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-06-14

Drug Details

Active Ingredients

IngredientStrength
ARSENIC TRIOXIDE30 [hp_X]/mL

OpenFDA Data

SPL SET ID:96035891-aea3-4138-bb26-801ad819f639
Manufacturer
UNII
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.