What is NDC 57687-352?

57687-352 is the product NDC for Bach Letting Go, Ulmus procera flowering twig 5 [hp_X]/.095mL + 2 more ingredients solution, listed with the FDA by Nelson Bach USA Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bach Letting Go (Elm, Red Chestnut, Walnut).

What is the active ingredient?

Ulmus procera flowering twig, Aesculus carnea flower, Juglans regia flowering top.

Nelson Bach USA Ltd, NDC labeler code 57687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bach Letting Go?

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.

Bach Letting Go NDC 57687-352 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)57687-352Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57687-0352Add 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
57687-352-20	5768703522057687035220	1 BOTTLE, DROPPER in 1 CARTON (57687-352-20) / 20 mL in 1 BOTTLE, DROPPERMarketed from Oct 9, 2026

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): Bach Letting Go
Generic name (nonproprietary): elm, red chestnut, walnut
Active ingredients: Ulmus procera flowering twig — 5 [hp_X]/.095mLAesculus carnea flower — 5 [hp_X]/.095mLJuglans regia flowering top — 5 [hp_X]/.095mL
Dosage form: Solution
Route: Oral
Labeler: Nelson Bach USA LtdNDC labeler code 57687
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 9, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 57687-352_5a6e9071-1bd5-de7e-e063-6294a90a8a77SPL ID 5a6e9071-1bd5-de7e-e063-6294a90a8a77

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

N457687035220 followed by a unit qualifier and the quantity

Package 57687-0352-20. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 57687-352

What is NDC 57687-352?: 57687-352 is the product NDC for Bach Letting Go, Ulmus procera flowering twig 5 [hp_X]/.095mL + 2 more ingredients solution, listed with the FDA by Nelson Bach USA Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bach Letting Go (Elm, Red Chestnut, Walnut).
What is the active ingredient?: Ulmus procera flowering twig, Aesculus carnea flower, Juglans regia flowering top.
Who is the labeler?: Nelson Bach USA Ltd, NDC labeler code 57687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bach Letting Go?: 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.

Bach Letting Go (Elm, red chestnut, walnut) NDC 57687-352