F19 Strng-Mnd NDC 63479-0619

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0619Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0619Add 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
63479-0619-1	63479061901	30 mL in 1 BOTTLE, GLASS (63479-0619-1)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): F19 Strng-MndSuffix: STRNG-MND
Generic name (nonproprietary): anacardium orientale, arnica montana, aurum metallicum, castanea sativa, citrus sinensis, crataegus monogyna, cytisus scoparius, dandelion, fagus sylvatica, fuchsia, gorse, hydrastis canadensis, ignatia amara, iron, kali phosphoricum, malus sylvestris, natrum muriaticum, paeonia californica, pomegranate, prunella vulgaris, rosa californica, sinapis arvensis, yarrow, yerba santa
Active ingredients: Arnica montana flower — 12 [hp_C]/mLIron — 12 [hp_C]/mLStrychnos ignatii seed — 20 [hp_X]/mLSodium chloride — 12 [hp_C]/mLPunica granatum flower — 12 [hp_C]/mLSinapis arvensis flowering/fruiting top — 12 [hp_C]/mLAchillea millefolium flower — 12 [hp_C]/mLPaeonia californica whole — 12 [hp_C]/mLMalus sylvestris flower — 12 [hp_C]/mLPrunella vulgaris flower — 12 [hp_C]/mLCastanea sativa flower — 12 [hp_C]/mLCitrus sinensis flower — 12 [hp_C]/mLTaraxacum officinale flowering top — 12 [hp_C]/mLUlex europaeus flower — 12 [hp_C]/mLPotassium phosphate, Dibasic — 12 [hp_C]/mLCytisus scoparius flower — 12 [hp_C]/mLEriodictyon californicum flowering top — 12 [hp_C]/mLCrataegus monogyna flower — 12 [hp_C]/mLHydrastis canadensis whole — 12 [hp_C]/mLSemecarpus anacardium juice — 12 [hp_X]/mLArnica montana — 12 [hp_X]/mLGold — 12 [hp_C]/mLRosa californica whole — 12 [hp_C]/mLFagus sylvatica flowering top — 12 [hp_C]/mLFuchsia magellanica whole — 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
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 63479-0619_0e7707c6-b7c8-adf7-e063-6294a90a60bcSPL ID 0e7707c6-b7c8-adf7-e063-6294a90a60bcSPL set ID bec4e5d7-d968-175b-e053-2a95a90a4e0aUNII OZ0E5Y15PZ, E1UOL152H7, 1NM3M2487K, 451W47IQ8X, D9B634V4GP, WWX61E1ZAK, YQR8R0SQEA, 38QL9598DU, 6ZJ8N1924Z, AT1FD041EF, YHZ719F7M3, H02N5LQ5F6, DQS85W46HV, 398DBS1PXN, CI71S98N1Z, 205JZ3JIKD, HKE3DK7994, NT52AMP29J, R763EBH88T, Y0F0BU8RDU, O80TY208ZW, 79Y1949PYO, H14X4P9EKJ, 21AF0IHY5U, J66MJH220LUPC 0818960011925
Pharmacologic class: Osmotic Laxative; Potassium Salt; Standardized Chemical Allergen

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

N463479061901 followed by a unit qualifier and the quantity

Package 63479-0619-01. 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: feeling overwhelmed* mental fatigue* weak memory* muscle tension* low-spirits* *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)