F25 Lf-Chngs (agrimony flower) NDC 63479-0625

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0625Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0625Add 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
63479-0625-1	63479062501	30 mL in 1 BOTTLE, GLASS (63479-0625-1)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): F25 Lf-ChngsSuffix: LF-CHNGS
Generic name (nonproprietary): agrimony flower
Active ingredients: Arsenic trioxide — 30 [hp_C]/mLLavandula angustifolia subsp. Angustifolia flower — 12 [hp_C]/mLSalix alba flowering top — 12 [hp_C]/mLArtemisia tridentata whole — 12 [hp_C]/mLRanunculus bulbosus whole — 12 [hp_C]/mLDieffenbachia seguine — 4 [hp_X]/mLRosa californica whole — 12 [hp_C]/mLMatricaria chamomilla flowering top — 12 [hp_C]/mLAesculus hippocastanum flower — 12 [hp_C]/mLCapsicum — 12 [hp_C]/mLLarrea tridentata whole — 12 [hp_C]/mLSalvia officinalis flowering top — 12 [hp_C]/mLCalluna vulgaris flowering top — 12 [hp_C]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLPenstemon davidsonii whole — 12 [hp_C]/mLLonicera caprifolium flower — 12 [hp_C]/mLGossypium herbaceum flower — 12 [hp_C]/mLEschscholzia californica flower — 12 [hp_C]/mLHylotelephium telephium whole — 12 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mLHelianthus annuus flowering top — 12 [hp_C]/mLCalochortus tolmiei whole — 12 [hp_C]/mLLawsonia inermis flowering top — 12 [hp_C]/mLAgrimonia eupatoria flower — 12 [hp_C]/mLArnica montana flower — 12 [hp_C]/mLFagus sylvatica flowering top — 12 [hp_C]/mLJuglans regia flowering top — 12 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLIpomoea purpurea top — 12 [hp_C]/mLPetunia axillaris whole — 12 [hp_C]/mLPlantago major — 4 [hp_X]/mLSilicon dioxide — 12 [hp_C]/mLMalva neglecta whole — 12 [hp_C]/mLPrunella vulgaris flower — 12 [hp_C]/mLPassiflora incarnata flowering top — 4 [hp_X]/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)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 63479-0625_0e771c1f-597e-e177-e063-6394a90a0b89SPL ID 0e771c1f-597e-e177-e063-6394a90a0b89SPL set ID bf3c7a21-0e4e-6395-e053-2a95a90a7156UNII S7V92P67HO, 19AH1RAF4M, XBP5X7E70R, 45E08M336T, AEQ8NXJ0MB, 01800C6E6B, H14X4P9EKJ, 3VNC7T6Z02, KK0Z92II8M, 00UK7646FG, B755J144H1, 48JCS720FN, D9PC510CQV, 269XH13919, 8K9DCX606Z, 5N1WD9784U, CVM893280N, 7JX5YDQ0D6, PH797NEU5T, QDL83WN8C2, BKJ0J3D1BP, 831MXG026J, UF2093XE64, 5811MI029U, OZ0E5Y15PZ, 21AF0IHY5U, 3BA2N709NG, VSW71SS07I, XMQ0V9812O, B7U2BWH3OT, W2469WNO6U, ETJ7Z6XBU4, S0QQA41760, AT1FD041EF, CLF5YFS11OUPC 0818960011987
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

N463479062501 followed by a unit qualifier and the quantity

Package 63479-0625-01. 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: despair* digestive discomfort* *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)