Dust Mix Antigen NDC 43406-0140

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0140Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0140Add 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
43406-0140-1	43406014001	30 mL in 1 BOTTLE, DROPPER (43406-0140-1)Marketed from Jul 12, 2012

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): Dust Mix Antigen
Generic name (nonproprietary): antimon tart, arsenicum alb, blatta or, bromium, calc carb, cimex, drosera, hepar sulph calc, ictodes foetida, lycopodium, phos, pulsatilla, silicea terra, tabacum fumus
Active ingredients: Antimony potassium tartrate — 30 [hp_C]/mLArsenic trioxide — 30 [hp_C]/mLBlatta orientalis — 30 [hp_C]/mLBromine — 30 [hp_C]/mLOyster shell calcium carbonate, Crude — 30 [hp_C]/mLCimex lectularius — 30 [hp_C]/mLDrosera rotundifolia — 30 [hp_C]/mLCalcium sulfide — 30 [hp_C]/mLSymplocarpus foetidus root — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLPulsatilla vulgaris — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLTobacco smoke — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 12, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Insect Proteins (Chemical structure)
Identifiers: Product ID 43406-0140_ec89c2e9-8a1e-4a93-a4cf-b7ed7bb27e76SPL ID ec89c2e9-8a1e-4a93-a4cf-b7ed7bb27e76SPL set ID 8dab4b4a-6fa8-4258-adc1-f8c634e2030bUNII DL6OZ476V3, S7V92P67HO, 535787266D, SBV4XY874G, 2E32821G6I, W66P4K3SGW, QR44N9XPJQ, 1MBW07J51Q, R88254608W, C88X29Y479, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4, 9BPR10844HUPC 0877730001252
Pharmacologic class: Non-Standardized Insect Allergenic Extract

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

N443406014001 followed by a unit qualifier and the quantity

Package 43406-0140-01. 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 Dec 21, 2018.

Indications (excerpt from the label)

USES: Temporarily relieves symptoms associated with allergic responses to dust.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)