What is NDC 68229-100?

68229-100 is the product NDC for Skin Tag Relief (thuja occidentalis leafy twig), Thuja occidentalis leafy twig 6 [hp_X]/10mL oil, listed with the FDA by Quest Products, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Skin Tag Relief (Thuja Occidentalis Leafy Twig).

Quest Products, Inc., NDC labeler code 68229. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Skin Tag 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.

Skin Tag Relief NDC 68229-100 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68229-100Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68229-0100Add 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
68229-100-02	68229010002	1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) / 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01)Marketed from May 21, 2013
68229-100-04	68229010004	1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-04) / 12.5 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-03)Marketed from May 23, 2022

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): Skin Tag Relief
Generic name (nonproprietary): thuja occidentalis leafy twig
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/10mL
Dosage form: Oil
Route: Topical
Labeler: Quest Products, Inc.NDC labeler code 68229
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 21, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 68229-100_262e23fb-5ad8-bbde-e063-6394a90ab37bSPL ID 262e23fb-5ad8-bbde-e063-6394a90ab37bSPL set ID 98fb9d4a-d0d2-425b-878b-927eebf53067UNII 1NT28V9397

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

NDC on a medical claim

N468229010002 followed by a unit qualifier and the quantity

Package 68229-0100-02. 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 Nov 5, 2024.

Indications (excerpt from the label)

Uses Symptomatic treatment of Skin Tags.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68229-100

What is NDC 68229-100?: 68229-100 is the product NDC for Skin Tag Relief (thuja occidentalis leafy twig), Thuja occidentalis leafy twig 6 [hp_X]/10mL oil, listed with the FDA by Quest Products, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Skin Tag Relief (Thuja Occidentalis Leafy Twig).
What is the active ingredient?: Thuja occidentalis leafy twig.
Who is the labeler?: Quest Products, Inc., NDC labeler code 68229. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Skin Tag 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.

Skin Tag Relief (Thuja occidentalis leafy twig) NDC 68229-100