What is NDC 17312-170?

17312-170 is the product NDC for Chronic Fatigue Therapy, Scutellaria lateriflora 6 [hp_X]/1 + 8 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Chronic Fatigue Therapy (Epinephrine, Gold, Chelidonium majus, Echinacea, Ginkgo, Helleborus niger, Phosphoric acid, Scutellaria lateriflora, Thuja occidentalis).

What is the active ingredient?

Scutellaria lateriflora, Thuja occidentalis leafy twig, Ginkgo, Chelidonium majus, Epinephrine, Phosphoric acid, Echinacea, Unspecified, Gold, Helleborus niger root.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Chronic Fatigue Therapy?

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.

Chronic Fatigue Therapy NDC 17312-170

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-170Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0170Add 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
17312-170-14	1731201701417312017014	1 BOTTLE in 1 PACKAGE (17312-170-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Aug 20, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Chronic Fatigue Therapy
Generic name (nonproprietary): epinephrine, gold, chelidonium majus, echinacea, ginkgo, helleborus niger, phosphoric acid, scutellaria lateriflora, thuja occidentalis
Active ingredients: Scutellaria lateriflora — 6 [hp_X]/1Thuja occidentalis leafy twig — 6 [hp_X]/1Ginkgo — 3 [hp_X]/1Chelidonium majus — 6 [hp_X]/1Epinephrine — 7 [hp_X]/1Phosphoric acid — 6 [hp_X]/1Echinacea, Unspecified — 3 [hp_X]/1Gold — 8 [hp_X]/1Helleborus niger root — 6 [hp_X]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 20, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 17312-170_4604f3de-7763-ddaa-e063-6394a90a78d0SPL ID 4604f3de-7763-ddaa-e063-6394a90a78d0SPL set ID 751334b8-f21b-3f94-e053-2a91aa0a9bb9UNII 7BP4DH5PDC, 1NT28V9397, 19FUJ2C58T, 7E889U5RNN, YKH834O4BH, E4GA8884NN, 4N9P6CC1DX, 79Y1949PYO, 608DGJ6815UPC 0858961001709
Pharmacologic class: Catecholamine; Standardized Chemical Allergen; 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

N417312017014 followed by a unit qualifier and the quantity

Package 17312-0170-14. 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 Dec 15, 2025.

Indications (excerpt from the label)

Uses According to homeopathic indications, these ingredients provide temporary relief from symptoms such as: • Fatigue • Memory loss • Sleeplessness • Weakness • Weariness • Muscle pain after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. 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 17312-170

What is NDC 17312-170?: 17312-170 is the product NDC for Chronic Fatigue Therapy, Scutellaria lateriflora 6 [hp_X]/1 + 8 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Chronic Fatigue Therapy (Epinephrine, Gold, Chelidonium majus, Echinacea, Ginkgo, Helleborus niger, Phosphoric acid, Scutellaria lateriflora, Thuja occidentalis).
What is the active ingredient?: Scutellaria lateriflora, Thuja occidentalis leafy twig, Ginkgo, Chelidonium majus, Epinephrine, Phosphoric acid, Echinacea, Unspecified, Gold, Helleborus niger root.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chronic Fatigue Therapy?: 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.