Bach Original Flower Remedies Rock Rose NDC 57687-225

NDC codes

FDA NDC Directory

Product NDC (as listed)57687-225Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57687-0225Add 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
57687-225-10	57687022510	1 BOTTLE, DROPPER in 1 CARTON (57687-225-10) / 10 mL in 1 BOTTLE, DROPPERMarketed from Sep 20, 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): Bach Original Flower Remedies Rock Rose
Generic name (nonproprietary): helianthemum nummularium
Active ingredients: Helianthemum nummularium flower — 5 [hp_X]/.095mL
Dosage form: Solution
Route: Oral
Labeler: Nelson Bach USA Limited
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 20, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 57687-225_ea240330-bb55-4970-e053-2a95a90aef97SPL ID ea240330-bb55-4970-e053-2a95a90aef97SPL set ID ea240330-bb54-4970-e053-2a95a90aef97UNII 51BRR32WPPUPC 0741273402039

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

N457687022510 followed by a unit qualifier and the quantity

Package 57687-0225-10. 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 Oct 3, 2022.

Indications (excerpt from the label)

Use For relief of naturally occurring simple nervous tension

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)