F15 Mnd-Mmry NDC 63479-0615

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0615Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0615Add 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
63479-0615-1	63479061501	30 mL in 1 BOTTLE, GLASS (63479-0615-1)Marketed from Mar 12, 1996

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): F15 Mnd-MmrySuffix: MND-MMRY
Generic name (nonproprietary): agnus castus, allegheny monkeyflower, anacardium orientale, arnica montana, arnica montana flower, banana, comfrey, calochortus gunnisonii, citrus paradisi, cornus nuttallii, ehrendorferia chrysantha, melilotus officinalis, myosotis sylvatica, ignatia amara, kali bromatum, lac caninum, ornithogalum umbellatum, peppermint, phosphoricum acidum, phosphorus, pinus sylvestris, ranunculus bulbosus, rudbeckia hirta, saguaro, toxicodendron diversilobum, yarrow, yerba santa, zinnia elegans
Active ingredients: Symphytum officinale whole — 30 [hp_C]/mLZinnia elegans whole — 30 [hp_C]/mLPeppermint — 30 [hp_C]/mLSemecarpus anacardium juice — 12 [hp_X]/mLMusa x paradisiaca flower — 30 [hp_C]/mLArnica montana — 120 [hp_C]/mLStrychnos ignatii seed — 60 [hp_C]/mLCalochortus gunnisonii whole — 30 [hp_C]/mLCitrus paradisi whole — 30 [hp_C]/mLMimulus ringens whole — 30 [hp_C]/mLRanunculus bulbosus whole — 30 [hp_C]/mLEhrendorferia chrysantha whole — 30 [hp_C]/mLChaste tree — 6 [hp_X]/mLArnica montana flower — 30 [hp_C]/mLRudbeckia hirta whole — 30 [hp_C]/mLPotassium bromide — 10 [hp_X]/mLAchillea millefolium flower — 30 [hp_C]/mLCornus nuttallii whole — 30 [hp_C]/mLToxicodendron diversilobum whole — 30 [hp_C]/mLPhosphoric acid — 10 [hp_X]/mLOrnithogalum umbellatum flowering top — 30 [hp_C]/mLPhosphorus — 12 [hp_X]/mLMyosotis sylvatica flowering top — 30 [hp_C]/mLMelilotus officinalis top — 30 [hp_C]/mLCanis lupus familiaris milk — 10 [hp_X]/mLCarnegiea gigantea flower — 30 [hp_C]/mLEriodictyon californicum flowering top — 30 [hp_C]/mLPinus sylvestris flowering top — 30 [hp_C]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 12, 1996
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 63479-0615_0e76f0d9-0aca-e097-e063-6394a90adba2SPL ID 0e76f0d9-0aca-e097-e063-6394a90adba2SPL set ID bf3bbec4-f9e0-5a2d-e053-2a95a90ab153UNII H8FJJ6KX5Y, 70TF95C8U7, V95R5KMY2B, Y0F0BU8RDU, DG5B0M0NGY, O80TY208ZW, 1NM3M2487K, H4ORZ75P00, W4KH5N2DCK, AEQ8NXJ0MB, 68HKD4QMJR, 433OSF3U8A, OZ0E5Y15PZ, 5W5Y77N8W9, OSD78555ZM, YQR8R0SQEA, F34859WS62, 9211E5735B, E4GA8884NN, CZD6M4PY4B, 27YLU75U4W, 2MBR3KL7IN, GM6P02J2DX, G39P120JQT, Z54WN9192C, HKE3DK7994, 2HEM73YI9I
Pharmacologic class: Non-Standardized Food 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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479061501 followed by a unit qualifier and the quantity

Package 63479-0615-01. 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 8, 2024.

Indications (excerpt from the label)

Uses: For temporary relief of minor: absence of mind* painful reflections* grief* headache* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)