E.O.L.

Product NDC
57520-0969
11-digit product format
575200969
Labeler code
57520
Product ID
57520-0969_59eb50e7-8121-468f-a1ae-6289638c1868
Type
HUMAN OTC DRUG
Nonproprietary name
Cholesterinum, Stillingia sylvatica, Zincum gluconicum, Thiaminum hydrochloricum, 5-hydroxytryptophan, Betain HCL, Biotin, Cholinum CoQ10, Dl-methionine, L-alanine, L-cysteine, L-cystine, L-glutamic acid, L-glutamine, L-methionine, L-serine, Lysine, PABA, Potassium gluconate,
Dosage form
LIQUID
Route
ORAL
Labeler
Apotheca Company
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-12-29
Marketing end
2022-09-24
Substance
AESCULUS HIPPOCASTANUM FLOWER; ALANINE; AMINOBENZOIC ACID; BETAINE HYDROCHLORIDE; BIOTIN; CHOLECALCIFEROL; CHOLESTEROL; CHOLINE HYDROXIDE; COPPER; CYSTEINE; CYSTINE; GLUTAMIC ACID; ILEX AQUIFOLIUM FLOWERING TOP; LYSINE; MALUS SYLVESTRIS FLOWER; METHIONINE; OXITRIPTAN; POTASSIUM GLUCONATE; RACEMETHIONINE; SELENIUM; SELENIUM DIOXIDE; SERINE; STILLINGIA SYLVATICA ROOT; SUS SCROFA THYMUS; THIAMINE HYDROCHLORIDE; THYROID, PORCINE; UBIDECARENONE; ZINC GLUCONATE
Active strength
30 [hp_C]/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_X]/mL; [hp_C]/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
Pharmacologic classes
Amino Acid [EPC], Amino Acids [CS], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Methylating Activity [MoA], Methylating Agent [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Vitamin B Complex Member [EPC], Vitamin B Complex [CS], Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57520-0969-12022-05-23C16284748780-19d75b9d0-84e8-f424-e053-dadaa90a57cee0985eba-b358-4d9f-be90-a1ed73a95039
57520-0969-12020-01-31C16284748780-19d75b9d0-84e8-f424-e053-dadaa90a57cee0985eba-b358-4d9f-be90-a1ed73a95039

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57520-0969-15752009690160 mL in 1 BOTTLE, DROPPER (57520-0969-1) 60 ml2011-12-292022-09-24NoNoCurrent