Anxiolix NDC 61657-0006

NDC codes

FDA NDC Directory

Product NDC (as listed)61657-0006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61657-0006Add 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
61657-0006-1	61657000601	30 mL in 1 BOTTLE, DROPPER (61657-0006-1)Marketed from Jun 1, 2011

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): Anxiolix
Generic name (nonproprietary): arsenicum album ,scutellaria lateriflora,phosphorus,lachesis mutus,pulsatilla,passiflora incarnata,aconite,valeriana officinalis,calcarea carbonica,ignatia amara
Active ingredients: Arsenic trioxide — 12 [hp_X]/30mLScutellaria lateriflora — 3 [hp_X]/30mLPhosphorus — 12 [hp_X]/30mLLachesis muta venom — 15 [hp_X]/30mLPulsatilla vulgaris — 12 [hp_X]/30mLPassiflora incarnata flowering top — 3 [hp_X]/30mLAconitum napellus — 12 [hp_X]/30mLValerian — 3 [hp_X]/30mLOyster shell calcium carbonate, Crude — 12 [hp_X]/30mLStrychnos ignatii seed — 12 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: White Manufacturing Inc. DBA Micro West
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 61657-0006_b9708571-5b82-4644-e053-2995a90a6a12SPL ID b9708571-5b82-4644-e053-2995a90a6a12SPL set ID 69660f20-c9ba-4b43-bc85-0fab3ff68c61UNII S7V92P67HO, 7BP4DH5PDC, 27YLU75U4W, VSW71SS07I, I76KB35JEV, CLF5YFS11O, U0NQ8555JD, JWF5YAW3QW, 2E32821G6I, 1NM3M2487K

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

N461657000601 followed by a unit qualifier and the quantity

Package 61657-0006-01. 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 Jan 21, 2021.

Indications (excerpt from the label)

INDICATIONS INDICATIONS : FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)