Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Anxiolix NDC 61657-0006
Arsenic trioxide 12 [hp_X]/30mL + 9 more ingredients · Liquid · Oral · White Manufacturing Inc. DBA Micro West
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 61657-0006-1 | 6165700060161657000601 | 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 WestNDC labeler code 61657
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- 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
N461657000601followed by a unit qualifier and the quantityPackage 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 .
Indications (excerpt from the label)
INDICATIONS INDICATIONS : FOR THE TEMPORARY RELIEF OF ANXIETY, SLEEPLESSNESS, NERVOUSNESS
Excerpt only. Read the full label for complete information.
About NDC 61657-0006
- What is NDC 61657-0006?
- 61657-0006 is the product NDC for Anxiolix, Arsenic trioxide 12 [hp_X]/30mL + 9 more ingredients liquid, listed with the FDA by White Manufacturing Inc. DBA Micro West. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Anxiolix (Arsenicum album ,Scutellaria lateriflora,Phosphorus,Lachesis mutus,Pulsatilla,Passiflora incarnata,Aconite,Valeriana officinalis,Calcarea carbonica,Ignatia amara).
- What is the active ingredient?
- Arsenic trioxide, Scutellaria lateriflora, Phosphorus, Lachesis muta venom, Pulsatilla vulgaris, Passiflora incarnata flowering top, Aconitum napellus, Valerian, Oyster shell calcium carbonate, Crude, Strychnos ignatii seed.
- Who is the labeler?
- White Manufacturing Inc. DBA Micro West, NDC labeler code 61657. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Anxiolix?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.