Energy Complex NDC 73162-0003

NDC codes

FDA NDC Directory

Product NDC (as listed)73162-0003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73162-0003Add 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
73162-0003-1	73162000301	30 mL in 1 BOTTLE, DROPPER (73162-0003-1)Marketed from Feb 27, 2020

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): Energy Complex
Generic name (nonproprietary): echinacea (angustifolia), lappa major, solidago virgaurea, taraxacum officinale, adrenalinum, aloe, arsenicum album, baptisia tinctoria, berberis aquifolium, berberis vulgaris, bryonia (alba), chelidonium majus, crotalus horridus, digitalis purpurea, ferrum metallicum, glonoinum, glycyrrhiza glabra, hydrocotyle asiatica, iodium, iris versicolor, lachesis mutus, lycopodium clavatum, natrum muriaticum, nux vomica, rhus tox, ruta graveolens, thuja occidentalis, thyroidinum (bovine)
Active ingredients: Echinacea angustifolia whole — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLEpinephrine — 15 [hp_X]/mLAloe — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLBaptisia tinctoria root — 15 [hp_X]/mLMahonia aquifolium root bark — 15 [hp_X]/mLBerberis vulgaris root bark — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLChelidonium majus whole — 15 [hp_X]/mLCrotalus horridus horridus venom — 15 [hp_X]/mLDigitalis — 15 [hp_X]/mLIron — 15 [hp_X]/mLNitroglycerin — 15 [hp_X]/mLGlycyrrhiza glabra — 15 [hp_X]/mLCentella asiatica — 15 [hp_X]/mLIodine — 15 [hp_X]/mLIris versicolor root — 15 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mLLycopodium clavatum spore — 15 [hp_X]/mLSodium chloride — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLToxicodendron pubescens leaf — 15 [hp_X]/mLRuta graveolens flowering top — 15 [hp_X]/mLThuja occidentalis leafy twig — 15 [hp_X]/mLThyroid, Bovine — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Health Masters LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 27, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 73162-0003_879a2cdd-bfcc-4711-a47d-d72cc8d68785SPL ID 879a2cdd-bfcc-4711-a47d-d72cc8d68785SPL set ID 9286ca29-8190-4867-9231-b0d68180cb10UNII VB06AV5US8, 597E9BI3Z3, 5405K23S50, 39981FM375, YKH834O4BH, V5VD430YW9, S7V92P67HO, 5EF0HWI5WU, VZJ9F3C3SB, 1TH8Q20J0U, T7J046YI2B, 7E889U5RNN, YHA2XLJ956, F1T8QT9U8B, E1UOL152H7, G59M7S0WS3, 2788Z9758H, 7M867G6T1U, 9679TC07X4, X43D4L3DQC, VSW71SS07I, C88X29Y479, 451W47IQ8X, 269XH13919, 6IO182RP7A, N94C2U587S, 1NT28V9397, MN18OTN73W
Pharmacologic class: Catecholamine; Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic 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

N473162000301 followed by a unit qualifier and the quantity

Package 73162-0003-01. 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 Jan 22, 2024.

Indications (excerpt from the label)

INDICATIONS: Formulated for symptoms associated with low energy, fatigue and mild stress.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)