NDC 61300-0001

MAX

Abrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger,

MAX is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Arize Supplements, Llc. The primary component is Artemisia Abrotanum Flowering Top; Semecarpus Anacardium Juice; Barium Chloride Dihydrate; Oyster Shell Calcium Carbonate, Crude; Tribasic Calcium Phosphate; Fucus Vesiculosus; Graphite; Helleborus Niger Root; Sus Scrofa Hypothalamus; Strychnos Ignatii Seed; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Claviceps Purpurea Sclerotium; Silicon Dioxide; Thymol; Sus Scrofa Thyroid; Onion; Pork Liver; Sus Scrofa Pancreas; Sus Scrofa Adrenal Gland; Melatonin; Niacinamide; Sus Scrofa Ovary; Sus Scrofa Testicle; Serotonin Hydrochloride; Thiamine Hydrochloride; Solidago Virgaurea Flowering Top.

Product ID61300-0001_381b38b5-bfeb-4c2a-b402-bcaa8a2fb5e6
NDC61300-0001
Product TypeHuman Otc Drug
Proprietary NameMAX
Generic NameAbrotanum (artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger,
Dosage FormSpray
Route of AdministrationORAL
Marketing Start Date2014-04-30
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameArize Supplements, LLC
Substance NameARTEMISIA ABROTANUM FLOWERING TOP; SEMECARPUS ANACARDIUM JUICE; BARIUM CHLORIDE DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; FUCUS VESICULOSUS; GRAPHITE; HELLEBORUS NIGER ROOT; SUS SCROFA HYPOTHALAMUS; STRYCHNOS IGNATII SEED; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; CLAVICEPS PURPUREA SCLEROTIUM; SILICON DIOXIDE; THYMOL; SUS SCROFA THYROID; ONION; PORK LIVER; SUS SCROFA PANCREAS; SUS SCROFA ADRENAL GLAND; MELATONIN; NIACINAMIDE; SUS SCROFA OVARY; SUS SCROFA TESTICLE; SEROTONIN HYDROCHLORIDE; THIAMINE HYDROCHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP
Active Ingredient Strength8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 Through2019-12-31

Packaging

NDC 61300-0001-1

30 mL in 1 BOTTLE, SPRAY (61300-0001-1)
Marketing Start Date2014-04-30
Marketing End Date2023-07-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61300-0001-1 [61300000101]

MAX SPRAY
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-04-30

Drug Details


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