What is NDC 17312-473?

17312-473 is the product NDC for Natural Relief Diarrhea Relief, Thuja occidentalis leafy twig 6 [hp_X]/1 + 6 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?

Natural Relief Diarrhea Relief (Aloe, Citrullus colocynthis, Croton tiglium, Lycopodium clavatum, Magnesium sulfate heptahydrate, Phosphoric acid, Thuja occidentalis).

What is the active ingredient?

Thuja occidentalis leafy twig, Phosphoric acid, Magnesium sulfate heptahydrate, Lycopodium clavatum spore, Croton tiglium seed, Citrullus colocynthis fruit pulp, Aloe.

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 Natural Relief Diarrhea Relief?

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.

Natural Relief Diarrhea Relief NDC 17312-473

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-473Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0473Add 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
17312-473-14	17312047314	1 BOTTLE in 1 PACKAGE (17312-473-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Apr 30, 2025

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): Natural Relief Diarrhea Relief
Generic name (nonproprietary): aloe, citrullus colocynthis, croton tiglium, lycopodium clavatum, magnesium sulfate heptahydrate, phosphoric acid, thuja occidentalis
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/1Phosphoric acid — 6 [hp_X]/1Magnesium sulfate heptahydrate — 6 [hp_X]/1Lycopodium clavatum spore — 6 [hp_X]/1Croton tiglium seed — 7 [hp_X]/1Citrullus colocynthis fruit pulp — 6 [hp_X]/1Aloe — 7 [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: Apr 30, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 17312-473_436de66a-ce49-e92c-e063-6394a90a2494SPL ID 436de66a-ce49-e92c-e063-6394a90a2494SPL set ID 436de0c5-acd6-e32b-e063-6394a90aa275UNII 1NT28V9397, E4GA8884NN, SK47B8698T, C88X29Y479, 0HK2GZK66E, 23H32AOH17, V5VD430YW9
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N417312047314 followed by a unit qualifier and the quantity

Package 17312-0473-14. 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 Nov 12, 2025.

Indications (excerpt from the label)

Uses* According to homeopathic indications these ingredients provide temporary relief from diarrhea symptoms 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 17312-473

What is NDC 17312-473?: 17312-473 is the product NDC for Natural Relief Diarrhea Relief, Thuja occidentalis leafy twig 6 [hp_X]/1 + 6 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?: Natural Relief Diarrhea Relief (Aloe, Citrullus colocynthis, Croton tiglium, Lycopodium clavatum, Magnesium sulfate heptahydrate, Phosphoric acid, Thuja occidentalis).
What is the active ingredient?: Thuja occidentalis leafy twig, Phosphoric acid, Magnesium sulfate heptahydrate, Lycopodium clavatum spore, Croton tiglium seed, Citrullus colocynthis fruit pulp, Aloe.
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 Natural Relief Diarrhea Relief?: 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.