What is NDC 53645-1983?

53645-1983 is the product NDC for Pulsatilla 6X (pulsatilla vulgaris), Pulsatilla vulgaris 6 [hp_X]/30mL liquid, 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?

Pulsatilla 6X (Pulsatilla vulgaris).

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 Pulsatilla 6X?

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.

Pulsatilla 6X NDC 53645-1983 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)53645-1983Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53645-1983Add 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
53645-1983-6	53645198306	30 mL in 1 BOTTLE (53645-1983-6)Marketed from Jul 21, 2026

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): Pulsatilla 6X
Generic name (nonproprietary): pulsatilla vulgaris
Active ingredients: Pulsatilla vulgaris — 6 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: True Botanica, LLCNDC labeler code 53645
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 21, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 53645-1983_3dead232-3111-e085-e063-6294a90a0926SPL ID 3dead232-3111-e085-e063-6294a90a0926SPL set ID 3dead232-3110-e085-e063-6294a90a0926UNII I76KB35JEV

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

N453645198306 followed by a unit qualifier and the quantity

Package 53645-1983-06. 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 Jul 21, 2026.

Indications (excerpt from the label)

Use: For temporary relief of a timid, weepy disposition, ear discharge, loss of smell. 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 53645-1983

What is NDC 53645-1983?: 53645-1983 is the product NDC for Pulsatilla 6X (pulsatilla vulgaris), Pulsatilla vulgaris 6 [hp_X]/30mL liquid, 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?: Pulsatilla 6X (Pulsatilla vulgaris).
What is the active ingredient?: Pulsatilla vulgaris.
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 Pulsatilla 6X?: 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.

Pulsatilla 6X (Pulsatilla vulgaris) NDC 53645-1983