Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Lactistat NDC 44911-0336
Arsenic trioxide 12 [hp_X]/mL + 10 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0336-1 | 4491103360144911033601 | 30 mL in 1 BOTTLE, DROPPER (44911-0336-1)Marketed from Mar 30, 2016 |
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)
- Lactistat
- Generic name (nonproprietary)
- arsenicum album, calcarea carbonica, cocculus indicus, graphites, hydrofluoricum acidum, lachesis mutus, lacticum acidum, rhus tox, ruta graveolens, sarcolacticum acidum, saccharum officinale
- Active ingredients
- Arsenic trioxide — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLHydrofluoric acid — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLLactic acid, Dl- — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLRuta graveolens flowering top — 12 [hp_X]/mLLactic acid, L- — 12 [hp_X]/mLSucrose — 30 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Energique, Inc.NDC labeler code 44911
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 44911-0336_49acc937-c24f-4f2a-b72c-e3457e0844e1SPL ID 49acc937-c24f-4f2a-b72c-e3457e0844e1SPL set ID 8dcc4a3a-9f21-4a77-ae42-b2c8283a076aUNII S7V92P67HO, 2E32821G6I, 810258W28U, 4QQN74LH4O, RGL5YE86CZ, VSW71SS07I, 3B8D35Y7S4, 6IO182RP7A, N94C2U587S, F9S9FFU82N, C151H8M554
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
N444911033601followed by a unit qualifier and the quantityPackage 44911-0336-01. 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: May temporarily relieve symptoms associated with lactic acid such as muscle weakness, muscle cramps and stiffness, and burning pain.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.
About NDC 44911-0336
- What is NDC 44911-0336?
- 44911-0336 is the product NDC for Lactistat, Arsenic trioxide 12 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Lactistat (Arsenicum Album, Calcarea Carbonica, Cocculus Indicus, Graphites, Hydrofluoricum Acidum, Lachesis Mutus, Lacticum Acidum, Rhus Tox, Ruta Graveolens, Sarcolacticum Acidum, Saccharum Officinale).
- What is the active ingredient?
- Arsenic trioxide, Oyster shell calcium carbonate, Crude, Anamirta cocculus seed, Graphite, Hydrofluoric acid, Lachesis muta venom, Lactic acid, Dl-, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Lactic acid, L-, Sucrose.
- Who is the labeler?
- Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Lactistat?
- 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.