Rubus NDC 60986-1011

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-1011Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-1011Add 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
60986-1011-3	60986101103	50 mL in 1 BOTTLE, GLASS (60986-1011-3)Marketed from Mar 1, 1992
60986-1011-4	60986101104	100 mL in 1 PACKAGE (60986-1011-4)Marketed from Mar 1, 1992

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): Rubus
Generic name (nonproprietary): rubus fruticosus, iris germanica, vaccinium myrtillus, syzygium jambolanum, okoubaka aubrevillei
Active ingredients: Blackberry — 2 [hp_X]/100mLIris x germanica root — 4 [hp_X]/100mLBilberry — 3 [hp_X]/100mLSyzygium cumini seed — 3 [hp_X]/100mLOkoubaka aubrevillei bark — 6 [hp_X]/100mL
Dosage form: Liquid
Route: Oral
Labeler: Marco Pharma International LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 1, 1992
Listing expires: Dec 31, 2027
Identifiers: Product ID 60986-1011_483b8e1e-a66f-9470-e063-6294a90af6a3SPL ID 483b8e1e-a66f-9470-e063-6294a90af6a3SPL set ID bcaf8cd2-3880-4dd7-9895-d33e63c1a229UNII 8A6OMU3I8L, 8N6VTJ9IWV, 9P2U39H18W, 820LSF646I, MK2074187Z

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

N460986101103 followed by a unit qualifier and the quantity

Package 60986-1011-03. 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 12, 2026.

Indications (excerpt from the label)

Suggested use Dosage: For acute conditions take 25 drops in water 3-4 times daily. For long-term usage, take 20 drops in water morning and evening. Dosage: For acute conditions take 25 drops in water 3-4 times daily. For long-term usage, take 20 drops in water morning and evening.

Excerpt only. Read the full label for complete information.

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