What is NDC 43742-1452?

43742-1452 is the product NDC for Elevate, Lycopodium clavatum spore 3 [hp_X]/mL + 23 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Elevate (Lycopodium Clavatum, Natrum Muriaticum, Sepia, Causticum, Phosphorus, Sulphur, 5-Hydroxytryptophan, Alumina, Silicea, Acetylcholine Chloride, Dopamine Hydrochloride, Norepinephrine (Bitartrate), 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)).

What is the active ingredient?

Lycopodium clavatum spore, Sodium chloride, Sepia officinalis juice, Causticum, Phosphorus, Sulfur, Oxitriptan, Aluminum oxide, Silicon dioxide, Acetylcholine chloride, Dopamine hydrochloride, Norepinephrine bitartrate, Phenethylamine hydrochloride, Serotonin hydrochloride, Adenosine cyclic phosphate, Sus scrofa cerebrum, Sus scrofa diencephalon, Sus scrofa umbilical cord, Pantothenic acid, Sus scrofa pineal gland, Lactic acid, L-, Alcaligenes faecalis, Salmonella enterica subsp. Enterica serovar enteritidis, Proteus vulgaris.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Elevate?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Elevate NDC 43742-1452 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1452Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1452Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43742-1452-1	4374214520143742145201	30 mL in 1 BOTTLE, DROPPER (43742-1452-1)Marketed from Mar 15, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Elevate
Generic name (nonproprietary): lycopodium clavatum, natrum muriaticum, sepia, causticum, phosphorus, sulphur, 5-hydroxytryptophan, alumina, silicea, acetylcholine chloride, dopamine hydrochloride, norepinephrine (bitartrate), 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)
Active ingredients: Lycopodium clavatum spore — 3 [hp_X]/mLSodium chloride — 3 [hp_X]/mLSepia officinalis juice — 3 [hp_X]/mLCausticum — 4 [hp_X]/mLPhosphorus — 4 [hp_X]/mLSulfur — 4 [hp_X]/mLOxitriptan — 6 [hp_X]/mLAluminum oxide — 8 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLAcetylcholine chloride — 8 [hp_X]/mLDopamine hydrochloride — 8 [hp_X]/mLNorepinephrine bitartrate — 8 [hp_X]/mLPhenethylamine hydrochloride — 8 [hp_X]/mLSerotonin hydrochloride — 8 [hp_X]/mLAdenosine cyclic phosphate — 10 [hp_X]/mLSus scrofa cerebrum — 10 [hp_X]/mLSus scrofa diencephalon — 10 [hp_X]/mLSus scrofa umbilical cord — 10 [hp_X]/mLPantothenic acid — 10 [hp_X]/mLSus scrofa pineal gland — 10 [hp_X]/mLLactic acid, L- — 10 [hp_X]/mLAlcaligenes faecalis — 30 [hp_C]/mLSalmonella enterica subsp. Enterica serovar enteritidis — 30 [hp_C]/mLProteus vulgaris — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Catecholamines (Chemical structure)Catecholamines (Chemical structure)Cholinergic Agonists (Mechanism)
Identifiers: Product ID 43742-1452_92d174e7-7f2b-405d-8b3d-9d79d6a34238SPL ID 92d174e7-7f2b-405d-8b3d-9d79d6a34238SPL set ID 5c0ff0d8-2db4-42c0-9b6d-572f9ad0c98bUNII C88X29Y479, 451W47IQ8X, QDL83WN8C2, DD5FO1WKFU, 27YLU75U4W, 70FD1KFU70, C1LJO185Q9, LMI26O6933, ETJ7Z6XBU4, AF73293C2R, 7L3E358N9L, IFY5PE3ZRW, VOF61XW69D, GKN429M9VS, E0399OZS9N, 4GB5DQR532, 23PJ4252VL, 118OYG6W3H, 19F5HK2737, 050QZ2EDK7, F9S9FFU82N, 05KB30NGW2, Y3V16D4PV4, 11T9HCO30OUPC 0810151881454
Pharmacologic class: Catecholamine; Cholinergic Receptor Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443742145201 followed by a unit qualifier and the quantity

Package 43742-1452-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 11, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • feelings of helplessness • sadness • difficulty sleeping • difficulty concentrating • irritability • loss of appetite • self loathing These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43742-1452

What is NDC 43742-1452?: 43742-1452 is the product NDC for Elevate, Lycopodium clavatum spore 3 [hp_X]/mL + 23 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Elevate (Lycopodium Clavatum, Natrum Muriaticum, Sepia, Causticum, Phosphorus, Sulphur, 5-Hydroxytryptophan, Alumina, Silicea, Acetylcholine Chloride, Dopamine Hydrochloride, Norepinephrine (Bitartrate), 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)).
What is the active ingredient?: Lycopodium clavatum spore, Sodium chloride, Sepia officinalis juice, Causticum, Phosphorus, Sulfur, Oxitriptan, Aluminum oxide, Silicon dioxide, Acetylcholine chloride, Dopamine hydrochloride, Norepinephrine bitartrate, Phenethylamine hydrochloride, Serotonin hydrochloride, Adenosine cyclic phosphate, Sus scrofa cerebrum, Sus scrofa diencephalon, Sus scrofa umbilical cord, Pantothenic acid, Sus scrofa pineal gland, Lactic acid, L-, Alcaligenes faecalis, Salmonella enterica subsp. Enterica serovar enteritidis, Proteus vulgaris.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Elevate?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.