Metab NDC 43742-1579

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1579Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1579Add 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
43742-1579-1	43742157901	30 mL in 1 BOTTLE, DROPPER (43742-1579-1)Marketed from Oct 7, 2019

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): Metab
Generic name (nonproprietary): ascorbicum acidum, cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, fumaricum acidum, germanium sesquioxide, iodium, magnesium metallicum, natrum oxalaceticum, pulsatilla (pratensis), thyroidinum (suis), vanadium metallicum
Active ingredients: Ascorbic acid — 6 [hp_X]/mLCysteine — 9 [hp_X]/mLManganese gluconate — 10 [hp_X]/mLOxogluric acid — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLIodine — 12 [hp_X]/mLMagnesium — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mLAnemone pratensis — 12 [hp_X]/mLSus scrofa thyroid — 12 [hp_X]/mLVanadium — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 7, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Ascorbic Acid (Chemical structure)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 43742-1579_a1663e3e-f20b-486d-a84b-ad32cff9f15dSPL ID a1663e3e-f20b-486d-a84b-ad32cff9f15dSPL set ID fbf89a37-dca2-4498-8866-234b033c5d42UNII PQ6CK8PD0R, K848JZ4886, 9YY2F980SV, 8ID597Z82X, 88XHZ13131, 96WE91N25T, 9679TC07X4, I38ZP9992A, 6CA025Y4FG, 8E272251DI, 6RV024OAUQ, 00J9J9XKDE
Pharmacologic class: Paramagnetic Contrast Agent; Vitamin C

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

N443742157901 followed by a unit qualifier and the quantity

Package 43742-1579-01. 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 12, 2023.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to headache, joint pain, sweating, congestion, and fatigue.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)