What is NDC 53645-1371?

53645-1371 is the product NDC for Aesculus 50X (aesculus hippocastanum whole), Aesculus hippocastanum whole 50 [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?

Aesculus 50X (Aesculus hippocastanum whole).

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 Aesculus 50X?

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.

Aesculus 50X NDC 53645-1371 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)53645-1371Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53645-1371Add 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
53645-1371-6	53645137106	30 mL in 1 BOTTLE (53645-1371-6)Marketed from Mar 17, 2025

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): Aesculus 50X
Generic name (nonproprietary): aesculus hippocastanum whole
Active ingredients: Aesculus hippocastanum whole — 50 [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: Mar 17, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 53645-1371_240fbc9b-f179-ddb1-e063-6294a90a9bf8SPL ID 240fbc9b-f179-ddb1-e063-6294a90a9bf8SPL set ID 240fb56a-6e0d-9020-e063-6394a90a5d04UNII 2331W47PSX

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

N453645137106 followed by a unit qualifier and the quantity

Package 53645-1371-06. 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 Mar 17, 2025.

Indications (excerpt from the label)

Use: Supports healthy teeth. For temporary relief of heavy feeling in the lower body. 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 53645-1371

What is NDC 53645-1371?: 53645-1371 is the product NDC for Aesculus 50X (aesculus hippocastanum whole), Aesculus hippocastanum whole 50 [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?: Aesculus 50X (Aesculus hippocastanum whole).
What is the active ingredient?: Aesculus hippocastanum whole.
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 Aesculus 50X?: 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.

Aesculus 50X (Aesculus hippocastanum whole) NDC 53645-1371