What is NDC 53645-1220?

53645-1220 is the product NDC for Thuja, Thuja occidentalis leafy twig 6 [hp_X]/23g globule, listed with the FDA by True Botanica, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

True Botanica, LLC, NDC labeler code 53645. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Thuja?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Thuja NDC 53645-1220 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)53645-1220Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53645-1220Add 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
53645-1220-2	53645122002	23 g in 1 BOTTLE (53645-1220-2)Marketed from Jun 21, 2013

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): Thuja
Generic name (nonproprietary): thuja
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/23g
Dosage form: Globule
Route: Oral
Labeler: True Botanica, LLCNDC labeler code 53645
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 21, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 53645-1220_b99bad22-372f-22f5-e053-2995a90a70f0SPL ID b99bad22-372f-22f5-e053-2995a90a70f0SPL set ID 34dea719-92b7-4b90-96fe-5270403e9b95UNII 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N453645122002 followed by a unit qualifier and the quantity

Package 53645-1220-02. 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 Jan 23, 2021.

Indications (excerpt from the label)

Use: For temporary relief of skin eruptions, exhaustion with anxiety. May also be used for standard homeopathic indications or as directed by your physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 53645-1220

What is NDC 53645-1220?: 53645-1220 is the product NDC for Thuja, Thuja occidentalis leafy twig 6 [hp_X]/23g globule, listed with the FDA by True Botanica, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Thuja.
What is the active ingredient?: Thuja occidentalis leafy twig.
Who is the labeler?: True Botanica, LLC, NDC labeler code 53645. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Thuja?: 1 other product NDC are listed under this name. See all Thuja NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Thuja NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Thujathuja occidentalis leafy twig	Thuja occidentalis leafy twig 3 [hp_X]/50mL	LiquidOral	PEKANA Naturheilmittel GmbH	59469-157	59469-0157-10