Elevate RXS

Product NDC

43742-0341

11-digit product format

437420341

Labeler code

43742

Product ID

43742-0341_f0476134-a410-4f6f-ae66-68d5f1ce5d32

Type

HUMAN OTC DRUG

Nonproprietary name

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

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-04-02

Marketing end

2020-12-11

Substance

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

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_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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record