Multi-Phenolic NDC 44911-0649

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0649Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0649Add 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
44911-0649-1	44911064901	30 mL in 1 BOTTLE, DROPPER (44911-0649-1)Marketed from Jan 11, 2022

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): Multi-Phenolic
Generic name (nonproprietary): mannose, 5-hydroxytryptophan, acetaldehyde, acetylcholine chloride, ascorbicum acidum, aspartame, butylated hydroxytoluene, caffeic acid, candida albicans, cinnamic acid, coniferyl alcohol, coumarinum, dopamine hydrochloride, estradiol, gaba (gamma-aminobutyric acid), gallicum acidum, histaminum hydrochloricum, hydrocortisone, indolum, l-dopa, l-phenylalanine, melatonin, menadione, norepinephrine (bitartrate), petroselinum crispum, phenyl isothiocyanate, piperine, progesterone, pyrrole, quercetin,
Active ingredients: Mannose, D- — 12 [hp_X]/mLOxitriptan — 12 [hp_X]/mLAcetaldehyde — 12 [hp_X]/mLAcetylcholine chloride — 12 [hp_X]/mLAscorbic acid — 12 [hp_X]/mLAspartame — 12 [hp_X]/mLButylated hydroxytoluene — 12 [hp_X]/mLCaffeic acid — 12 [hp_X]/mLCandida albicans — 12 [hp_X]/mLCinnamic acid — 12 [hp_X]/mLConiferyl alcohol — 12 [hp_X]/mLCoumarin — 12 [hp_X]/mLDopamine hydrochloride — 12 [hp_X]/mLEstradiol — 12 [hp_X]/mL.gamma.-aminobutyric acid — 12 [hp_X]/mLGallic acid monohydrate — 12 [hp_X]/mLHistamine dihydrochloride — 12 [hp_X]/mLHydrocortisone — 12 [hp_X]/mLIndole — 12 [hp_X]/mLLevodopa — 12 [hp_X]/mLPhenylalanine — 12 [hp_X]/mLMelatonin — 12 [hp_X]/mLMenadione — 12 [hp_X]/mLNorepinephrine bitartrate — 12 [hp_X]/mLPetroselinum crispum whole — 12 [hp_X]/mLPhenyl isothiocyanate — 12 [hp_X]/mLPiperine — 12 [hp_X]/mLProgesterone — 12 [hp_X]/mLPyrrole — 12 [hp_X]/mLQuercetin — 12 [hp_X]/mLRutin — 12 [hp_X]/mLSerotonin hydrochloride — 12 [hp_X]/mLTaurine — 12 [hp_X]/mLTyramine — 12 [hp_X]/mLChlorogenic acid — 16 [hp_X]/mLPhlorizin — 16 [hp_X]/mLMalvin — 12 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 11, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Aromatic (Chemical structure)Ascorbic Acid (Chemical structure)Catecholamines (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cholinergic Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)Estradiol Congeners (Chemical structure)Estrogen Receptor Agonists (Mechanism)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Progesterone (Chemical structure)
Identifiers: Product ID 44911-0649_6ec419e2-8fad-41b7-b9bd-5ddfc89ffab8SPL ID 6ec419e2-8fad-41b7-b9bd-5ddfc89ffab8SPL set ID 492b412a-01cc-48f2-bcdc-6fffcc651963UNII PHA4727WTP, C1LJO185Q9, GO1N1ZPR3B, AF73293C2R, PQ6CK8PD0R, Z0H242BBR1, 1P9D0Z171K, U2S3A33KVM, 4D7G21HDBC, U14A832J8D, E7SM92591P, A4VZ22K1WT, 7L3E358N9L, 4TI98Z838E, 2ACZ6IPC6I, 48339473OT, 3POA0Q644U, WI4X0X7BPJ, 8724FJW4M5, 46627O600J, 47E5O17Y3R, JL5DK93RCL, 723JX6CXY5, IFY5PE3ZRW, 1WZA4Y92EX, 0D58F84LSU, U71XL721QK, 4G7DS2Q64Y, 86S1ZD6L2C, 9IKM0I5T1E, 5G06TVY3R7, GKN429M9VS, 1EQV5MLY3D, X8ZC7V0OX3, 318ADP12RI, CU9S17279X, I9I120531L
Pharmacologic class: Aromatic Amino Acid; Catecholamine; Cholinergic Receptor Agonist; Corticosteroid; Estrogen; Non-Standardized Fungal Allergenic Extract; Progesterone; Vitamin C

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

N444911064901 followed by a unit qualifier and the quantity

Package 44911-0649-01. 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 Aug 23, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms associated with sensitivities to phenolic compounds such as rash, fatigue, and lack of concentration.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)