911 Adrenal Burnout and Fatigue NDC 57955-9994

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9994Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9994Add 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
57955-9994-2	57955999402	59 mL in 1 BOTTLE, SPRAY (57955-9994-2)Marketed from Oct 20, 2025

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): 911 Adrenal Burnout and Fatigue
Generic name (nonproprietary): aceticum ac, adrenalinum, adrenocorticotrophin (30x), aesculus hippocastanum, flos, alfalfa, alpha-lipoic ac, ambra, arg nit, avena sativa, bryonia, carboneum oxygenisatum, carpinus betulus, flos, dna, fumaricum acidum, gelsemium sempervirens, hepar sulphuris calcareum, hypothalamus, kali phosphoricum, lacticum acidum, lecithin, natrum muriaticum, oxalicum acidum, phosphoricum acidum, pituitarum posterium, sarcolacticum acidum, selenium metallicum, sepia, silicea, succinicum acidum and thyroidinum.
Active ingredients: Acetic acid — 10 [hp_X]/59mLEpinephrine — 10 [hp_X]/59mLCorticotropin — 30 [hp_X]/59mLAesculus hippocastanum flower — 10 [hp_X]/59mLAlfalfa — 10 [hp_X]/59mLAlpha lipoic acid — 10 [hp_X]/59mLAmbergris — 10 [hp_X]/59mLSilver nitrate — 10 [hp_X]/59mLAvena sativa flowering top — 10 [hp_X]/59mLBryonia alba root — 10 [hp_X]/59mLCarbon monoxide — 10 [hp_X]/59mLCarpinus betulus flowering top — 10 [hp_X]/59mLHerring sperm DNA — 10 [hp_X]/59mLFumaric acid — 10 [hp_X]/59mLGelsemium sempervirens root — 10 [hp_X]/59mLCalcium sulfide — 10 [hp_X]/59mLBos taurus hypothalamus — 10 [hp_X]/59mLDibasic potassium phosphate — 10 [hp_X]/59mLLactic acid, Dl- — 10 [hp_X]/59mLEgg phospholipids — 10 [hp_X]/59mLSodium chloride — 10 [hp_X]/59mLOxalic acid dihydrate — 10 [hp_X]/59mLPhosphoric acid — 10 [hp_X]/59mLSus scrofa pituitary gland, Posterior — 10 [hp_X]/59mLLactic acid, L- — 10 [hp_X]/59mLSelenium — 10 [hp_X]/59mLSepia officinalis juice — 10 [hp_X]/59mLSilicon dioxide — 10 [hp_X]/59mLSuccinic acid — 10 [hp_X]/59mLThyroid, Unspecified — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 8, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Adrenocorticotropic Hormone (Chemical structure)Catecholamines (Chemical structure)
Identifiers: Product ID 57955-9994_3d0df0e5-afcb-4b20-a54e-fbe7ee6234ddSPL ID 3d0df0e5-afcb-4b20-a54e-fbe7ee6234ddSPL set ID 21c6b6c1-e846-4f25-a1dc-02e79d1be756UNII Q40Q9N063P, YKH834O4BH, K0U68Q2TXA, KK0Z92II8M, DJO934BRBD, 73Y7P0K73Y, XTC0D02P6C, 95IT3W8JZE, MA9CQJ3F7F, T7J046YI2B, 7U1EE4V452, QOI241B01F, 51FI676N6F, 88XHZ13131, 639KR60Q1Q, 1MBW07J51Q, S6G2NLH4Y7, CI71S98N1Z, 3B8D35Y7S4, 1Z74184RGV, 451W47IQ8X, 0K2L2IJ59O, E4GA8884NN, E8S87O660T, F9S9FFU82N, H6241UJ22B, QDL83WN8C2, ETJ7Z6XBU4, AB6MNQ6J6L, 0B4FDL9I6P
Pharmacologic class: Adrenocorticotropic Hormone; Catecholamine; 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

N457955999402 followed by a unit qualifier and the quantity

Package 57955-9994-02. 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 Feb 26, 2026.

Indications (excerpt from the label)

Uses † for temporary relief of: physical fatigue mental and emotional fatigue nervous exhaustion sluggish mind poor concentration weariness confusion apathy irritability indifference body aches lack of focus eyes sensitive to light digestive symptoms caused by stress light-headed upon standing up † 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)