Kreosote NDC 85816-2227

NDC codes

FDA NDC Directory

Product NDC (as listed)85816-2227Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85816-2227Add 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
85816-2227-1	85816222701	30 mL in 1 BOTTLE, GLASS (85816-2227-1)Marketed from Jan 1, 2015
85816-2227-2	85816222702	500 mL in 1 BOTTLE, GLASS (85816-2227-2)Marketed from Jan 1, 2015

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): Kreosote
Generic name (nonproprietary): acid nit, belladonna, borax, chamomilla, kreosote, merc sol, staphysagria
Active ingredients: Sodium borate — 7 [hp_X]/mLAtropa belladonna — 7 [hp_X]/mLNitric acid — 7 [hp_X]/mLWood creosote — 7 [hp_X]/mLMercurius solubilis — 10 [hp_X]/mLChamomile — 7 [hp_X]/mLDelphinium staphisagria seed — 7 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BM Private Limited
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2027
Identifiers: Product ID 85816-2227_4ae55c0e-3e9a-703b-e063-6394a90a345aSPL ID 4ae55c0e-3e9a-703b-e063-6394a90a345aSPL set ID 3b3cb32b-e7e3-3455-e063-6394a90aaafbUNII 91MBZ8H3QO, WQZ3G9PF0H, 411VRN1TV4, 3JYG22FD73, 324Y4038G2, FGL3685T2X, 00543AP1JV

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

N485816222701 followed by a unit qualifier and the quantity

Package 85816-2227-01. 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 Feb 15, 2026.

Indications (excerpt from the label)

For detail, please read the enclosed package (product information leaflet)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)