F05 Slfstm NDC 63479-0605

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0605Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0605Add 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
63479-0605-1	63479060501	30 mL in 1 BOTTLE, GLASS (63479-0605-1)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): F05 SlfstmSuffix: SLFSTM
Generic name (nonproprietary): bulbous buttercup, centaury, ceratostigma willmottianum, jasminum officinale, lac caninum, larix decidua, lycopodium clavatum, asimina triloba, prickly pear, pulsatilla vulgaris, roundleaf mallow, saguaro, sunflower, trumpet vine, yellow jasmine
Active ingredients: Lycopodium clavatum spore — 12 [hp_C]/mLAsimina triloba whole — 12 [hp_C]/mLCarnegiea gigantea flower — 12 [hp_C]/mLHelianthus annuus flowering top — 12 [hp_C]/mLCentaurium erythraea flower — 12 [hp_C]/mLOpuntia ficus-indica flower — 12 [hp_C]/mLPulsatilla vulgaris whole — 12 [hp_C]/mLCampsis radicans flower — 12 [hp_C]/mLMalva neglecta whole — 12 [hp_C]/mLJasminum officinale flower — 12 [hp_C]/mLRanunculus bulbosus — 12 [hp_C]/mLCeratostigma willmottianum flower — 12 [hp_C]/mLGelsemium sempervirens root — 12 [hp_C]/mLCanis lupus familiaris milk — 12 [hp_C]/mLLarix decidua flowering top — 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 63479-0605_0e76f50e-2560-d499-e063-6394a90aa92eSPL ID 0e76f50e-2560-d499-e063-6394a90aa92eSPL set ID bca81c91-a949-326f-e053-2995a90a45bbUNII C88X29Y479, 06M320D5U9, Z54WN9192C, BKJ0J3D1BP, B204P54Z1F, 83YSP51SMA, I76KB35JEV, 9I1JVD2I03, S0QQA41760, 0Q8K841432, AEQ8NXJ0MB, TP69J995TW, 639KR60Q1Q, G39P120JQT, 9UMZ642257UPC 0818960011796

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

N463479060501 followed by a unit qualifier and the quantity

Package 63479-0605-01. 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: fatigue* loss of confidence* low-spiritedness* fear* nausea* apprehension* insomnia* *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)