What is NDC 59672-0916?

59672-0916 is the product NDC for No-Weak-Nails, Graphite 30 [hp_C]/1 + 2 more ingredients tablet, listed with the FDA by Miers Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

No-Weak-Nails (GRAPHITE, THUJA OCCIDENTALIS LEAFY TWIG, and SILICON DIOXIDE).

What is the active ingredient?

Graphite, Thuja occidentalis leafy twig, Silicon dioxide.

Miers Laboratories, NDC labeler code 59672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for No-Weak-Nails?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

No-Weak-Nails NDC 59672-0916 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59672-0916Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59672-0916Add 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
59672-0916-2	59672091602	1 BLISTER PACK in 1 CARTON (59672-0916-2) / 16 TABLET in 1 BLISTER PACKMarketed from Sep 15, 2014

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): No-Weak-Nails
Generic name (nonproprietary): graphite, thuja occidentalis leafy twig, and silicon dioxide
Active ingredients: Graphite — 30 [hp_C]/1Thuja occidentalis leafy twig — 30 [hp_C]/1Silicon dioxide — 30 [hp_C]/1
Dosage form: Tablet
Route: Oral
Labeler: Miers LaboratoriesNDC labeler code 59672
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 15, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 59672-0916_602d950e-0b4e-4be0-a84d-f459bd0c9aa3SPL ID 602d950e-0b4e-4be0-a84d-f459bd0c9aa3SPL set ID 9158cd3f-4c27-40e9-bc07-fd560375c3a1UNII 4QQN74LH4O, 1NT28V9397, ETJ7Z6XBU4

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459672091602 followed by a unit qualifier and the quantity

Package 59672-0916-02. 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 9, 2025.

Indications (excerpt from the label)

Uses Improves the strength and appearance of finger nails

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59672-0916

What is NDC 59672-0916?: 59672-0916 is the product NDC for No-Weak-Nails, Graphite 30 [hp_C]/1 + 2 more ingredients tablet, listed with the FDA by Miers Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: No-Weak-Nails (GRAPHITE, THUJA OCCIDENTALIS LEAFY TWIG, and SILICON DIOXIDE).
What is the active ingredient?: Graphite, Thuja occidentalis leafy twig, Silicon dioxide.
Who is the labeler?: Miers Laboratories, NDC labeler code 59672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for No-Weak-Nails?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.