Metalock

Product NDC
72190-0001
11-digit product format
721900001
Labeler code
72190
Product ID
72190-0001_60ad61f0-97ad-42cb-ab73-b9ff6ed00302
Type
HUMAN OTC DRUG
Nonproprietary name
Passiflora Incarnata, Chamomilla, Valeriana Officinalis, Fucus Officinalis, Agnus Castus, Kali Phosphoricum, Natrum Muriaticum, Nux Vomica, Phytolacca Decandra, Chelidonium Majus, Lycopodium Clavatum, Pituitarum Posterium (Bovine), Adrenocorticotrophin, Thyroidinum (Bovine), Thyroidinum (Ovine), Calcarea Carbonica, Carbo Vegetabilis, Magnesia Phosphorica, Natrum Phosphoricum, Ubidecarenonum, Graphites, Hypophysis Suis, Hypothalamus (Bovine), Placenta Totalis Suis, Argentum Nitricum, Berberis Vulgaris,
Dosage form
LIQUID
Route
ORAL
Labeler
Real Health Medical, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-04-04
Marketing end
2024-04-18
Substance
PASSIFLORA INCARNATA FLOWERING TOP; MATRICARIA CHAMOMILLA; VALERIAN; FUCUS VESICULOSUS; CHASTE TREE FRUIT; DIBASIC POTASSIUM PHOSPHATE; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; CHELIDONIUM MAJUS; LYCOPODIUM CLAVATUM SPORE; BOS TAURUS PITUITARY GLAND, POSTERIOR; CORTICOTROPIN; THYROID, BOVINE; THYROID, OVINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; UBIDECARENONE; GRAPHITE; SUS SCROFA PITUITARY GLAND; BOS TAURUS HYPOTHALAMUS; SUS SCROFA PLACENTA; SILVER NITRATE; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; DIGITALIS; IRIS VERSICOLOR ROOT; POTASSIUM CARBONATE; SODIUM CARBONATE; SODIUM SULFATE; ANEMONE PULSATILLA; TOXICODENDRON PUBESCENS LEAF; SCUTELLARIA LATERIFLORA; SEPIA OFFICINALIS JUICE; DATURA STRAMONIUM; SEMECARPUS ANACARDIUM JUICE; AGRIMONIA EUPATORIA FLOWER; CASTANEA SATIVA LEAF; CERATOSTIGMA WILLMOTTIANUM FLOWER; AESCULUS HIPPOCASTANUM FLOWER; CENTAURIUM ERYTHRAEA FLOWER
Active strength
3 [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_Q]/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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72190-0001-17219000010159 mL in 1 BOTTLE, DROPPER (72190-0001-1) 59 ml2019-04-040000-00-00NoNoCurrent