Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Lymphastat F NDC 44911-0708
Echinacea angustifolia whole 3 [hp_X]/mL + 11 more ingredients · Liquid · Oral · Energique, Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0708-1 | 44911070801 | 60 mL in 1 BOTTLE, DROPPER (44911-0708-1)Marketed from Mar 8, 2024 |
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)
- Lymphastat F
- Generic name (nonproprietary)
- echinacea (angustifolia), tabebuia impetiginosa, abies nigra, borax, lycopodium clavatum, nux vomica, phosphorus, pulsatilla (vulgaris), sepia, thuja occidentalis, skatolum, candida albicans
- Active ingredients
- Echinacea angustifolia whole — 3 [hp_X]/mLHandroanthus impetiginosus bark — 3 [hp_X]/mLPicea mariana resin — 12 [hp_X]/mLSodium borate — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLSkatole — 15 [hp_X]/mLCandida albicans — 30 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Energique, Inc
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
- Identifiers
- Product ID 44911-0708_2e00bd2f-3a46-46f6-bbe2-d034c79e7bacSPL ID 2e00bd2f-3a46-46f6-bbe2-d034c79e7bacSPL set ID 97467eb0-a08b-4223-b54a-af1d910577e8UNII VB06AV5US8, 6GLA1946WX, 71AOV0W131, 91MBZ8H3QO, C88X29Y479, 269XH13919, 27YLU75U4W, I76KB35JEV, QDL83WN8C2, 1NT28V9397, 9W945B5H7R, 4D7G21HDBCUPC 0363113701715
- Pharmacologic class
- Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant Allergenic Extract
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
N444911070801followed by a unit qualifier and the quantityPackage 44911-0708-01. 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)
USES: May temporarily relieve heartburn, bloating, itching, rash, burning on urination, fatigue, and apathy.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.