Elevate

Product NDC

43742-1036

Requested package NDC

43742-1036-1

11-digit product format

437421036

Labeler code

43742

Product ID

43742-1036_3a0fd953-cbb6-4652-a05c-93d38384d715

Type

HUMAN OTC DRUG

Nonproprietary name

Lycopodium Clavatum, Natrum Muriaticum, Sepia, Causticum, Phosphorus, Sulphur, 5-Hydroxytryptophan, Alumina, Silicea, Acetylcholine Chloride, Dopamine Hydrochloride, Norepinephrine, Phenylethylamine (Hydrochloride), Serotonin (Hydrochloride), Adenosinum Cyclophosphoricum, Cerebrum (Suis), Diencephalon (Suis), Funiculus Umbilicalis Suis, Pantothenic Acid, Pineal Gland (Suis), Sarcolacticum Acidum, Faecalis (Alkaligenes), Gaertner Bacillus (Bach), Proteus (Vulgaris)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-07-20

Marketing end

2024-02-04

Substance

ACETYLCHOLINE CHLORIDE; ADENOSINE CYCLIC PHOSPHATE; ALCALIGENES FAECALIS; ALUMINUM OXIDE; CAUSTICUM; DOPAMINE HYDROCHLORIDE; LACTIC ACID, L-; LYCOPODIUM CLAVATUM SPORE; NOREPINEPHRINE; OXITRIPTAN; PANTOTHENIC ACID; PHENETHYLAMINE HYDROCHLORIDE; PHOSPHORUS; PROTEUS VULGARIS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SEPIA OFFICINALIS JUICE; SEROTONIN HYDROCHLORIDE; SILICON DIOXIDE; SODIUM CHLORIDE; SULFUR; SUS SCROFA CEREBRUM; SUS SCROFA DIENCEPHALON; SUS SCROFA PINEAL GLAND; SUS SCROFA UMBILICAL CORD

Active strength

8 [hp_X]/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_C]/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

Pharmacologic classes

Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record