F09 Ltgo NDC 63479-0609

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0609Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0609Add 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
63479-0609-1	63479060901	30 mL in 1 BOTTLE, GLASS (63479-0609-1)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): F09 LtgoSuffix: LTGO
Generic name (nonproprietary): adelheid aqua, agrimony, malus sylvestris, arsenicum album, filaree, heather, horse chestnut, lachesis mutus, nasturtium, red horse chestnut, sepia, silicea, stramonium, verbena officinalis
Active ingredients: Arsenic trioxide — 12 [hp_C]/mLErodium cicutarium — 12 [hp_C]/mLCalluna vulgaris flowering top — 12 [hp_C]/mLAesculus hippocastanum flower — 12 [hp_C]/mLLachesis muta venom — 9 [hp_C]/mLVerbena officinalis flowering top — 12 [hp_C]/mLWater — 12 [hp_C]/mLAgrimonia eupatoria flower — 12 [hp_C]/mLTropaeolum majus flower — 12 [hp_C]/mLSepia officinalis juice — 12 [hp_C]/mLDatura stramonium — 9 [hp_C]/mLAesculus x carnea flower — 12 [hp_C]/mLSilicon dioxide — 9 [hp_C]/mLMalus sylvestris flower — 12 [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
Identifiers: Product ID 63479-0609_0e76f50e-2565-d499-e063-6394a90aa92eSPL ID 0e76f50e-2565-d499-e063-6394a90aa92eSPL set ID bd1e652f-b3a4-c5bd-e053-2995a90ae03fUNII S7V92P67HO, FJL3XFK3N8, D9PC510CQV, KK0Z92II8M, VSW71SS07I, 311PNK9CDZ, 059QF0KO0R, 5811MI029U, 7FV667B00B, QDL83WN8C2, G6W4F0V8Z3, 717DPT98VM, ETJ7Z6XBU4, 6ZJ8N1924ZUPC 0818960011833

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

N463479060901 followed by a unit qualifier and the quantity

Package 63479-0609-01. 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: feelings of anguish* worry* restlessness* inability to let go of obsessions* *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)