Allernest NDC 60986-1003

NDC codes

FDA NDC Directory

Product NDC (as listed)60986-1003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60986-1003Add 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
60986-1003-3	60986100303	50 mL in 1 BOTTLE, GLASS (60986-1003-3)Marketed from Feb 27, 2018
60986-1003-4	60986100304	100 mL in 1 BOTTLE, GLASS (60986-1003-4)Marketed from Feb 27, 2018

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): Allernest
Generic name (nonproprietary): formicum acidum, lachesis mutus, luffa operculata. petroleum, rhus toxicodebdron, aralai racemosa,galphimia glauca, thuja occidentalis, urtica dicica and cardiospermum
Active ingredients: Formic acid — 12 [hp_X]/mLLachesis muta venom — 8 [hp_X]/mLLuffa operculata fruit — 6 [hp_X]/mLKerosene — 6 [hp_X]/mLToxicodendron pubescens leaf — 6 [hp_X]/mLAralia racemosa root — 4 [hp_X]/mLGalphimia glauca flowering top — 4 [hp_X]/mLThuja occidentalis leafy twig — 4 [hp_X]/mLUrtica dioica — 4 [hp_X]/mLCardiospermum halicacabum flowering top — 3 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Marco Pharma International LLC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 18, 2011
Listing expires: Dec 31, 2027
Identifiers: Product ID 60986-1003_483c3446-1d4b-0503-e063-6394a90a4defSPL ID 483c3446-1d4b-0503-e063-6394a90a4defSPL set ID 97e4b6be-f93d-43de-a881-c27970201045UNII 0YIW783RG1, VSW71SS07I, C4MO6809HU, 1C89KKC04E, 6IO182RP7A, T90W4582DU, 93PH5Q8M7E, 1NT28V9397, 710FLW4U46, MZP2508BRR

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

N460986100303 followed by a unit qualifier and the quantity

Package 60986-1003-03. 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 Adults: in acute disorders, take 10 drops every 15 minutes on the tongue or with water until improvement if felt, then take 10 drops less frequently. To maintain balance, take 15 drops three times daily. Children receive 1/2 of the adult amount.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)