NDC codes

FDA NDC Directory
Product NDC (as listed)68466-2001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68466-2001Add 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 NDC11-digit (billing)PackageCopy
68466-2001-868466200108684662001081 TUBE in 1 CARTON (68466-2001-8) / 77 g in 1 TUBEMarketed from Oct 1, 2021

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)
Triflora Gel
Generic name (nonproprietary)
urtica dioica, toxicodendron pubescens leaf, ledum palustre twig
Active ingredients
Urtica dioica — 1 [hp_X]/77gToxicodendron pubescens leaf — 4 [hp_X]/77gLedum palustre twig — 2 [hp_X]/77g
Dosage form
Gel
Route
Topical, Topical
Labeler
Schwabe Mexico S.A. de C.V.NDC labeler code 68466
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 68466-2001_e3f082b2-ad1c-4ed8-a077-bb2bc4d2134dSPL ID e3f082b2-ad1c-4ed8-a077-bb2bc4d2134dSPL set ID a1c113ad-8c6c-4f19-b611-426e30f1db0eUNII 710FLW4U46, 6IO182RP7A, 877L01IZ0PUPC 0308078252971

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. Topical, Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468466200108 followed by a unit qualifier and the quantity

Package 68466-2001-08. 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 .

Indications (excerpt from the label)

Indications and Usage Temporarily relieves minor aches, pains, and joint/muscle stiffness associated with arthritis, rheumatism, simple backache, and tendinitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68466-2001

What is NDC 68466-2001?
68466-2001 is the product NDC for Triflora Gel, Urtica dioica 1 [hp_X]/77g + 2 more ingredients gel, listed with the FDA by Schwabe Mexico S.A. de C.V.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Triflora Gel (Urtica dioica, Toxicodendron pubescens leaf, Ledum palustre twig).
What is the active ingredient?
Urtica dioica, Toxicodendron pubescens leaf, Ledum palustre twig.
Who is the labeler?
Schwabe Mexico S.A. de C.V., NDC labeler code 68466. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triflora Gel?
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.

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