Asp NDC 43857-0547

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0547Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0547Add 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
43857-0547-1	43857054701	30 mL in 1 BOTTLE, DROPPER (43857-0547-1)Marketed from Mar 3, 2020

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): Asp
Generic name (nonproprietary): echinacea (angustifolia), tabebuia impetiginosa, hydrastis canadensis, glandula suprarenalis suis, thymus (suis), thyroidinum (suis), arsenicum album, bryonia (alba), cocculus indicus, colchicum autumnale, ledum palustre, mercurius cyanatus, natrum sulphuricum, pulsatilla (pratensis), sepia, silicea, aflatoxin (b1)
Active ingredients: Echinacea angustifolia whole — 3 [hp_X]/mLHandroanthus impetiginosus bark — 3 [hp_X]/mLGoldenseal — 5 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLSus scrofa thymus — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLColchicum autumnale bulb — 12 [hp_X]/mLLedum palustre twig — 12 [hp_X]/mLMercuric cyanide — 12 [hp_X]/mLSodium sulfate — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLAflatoxin b1 — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0547_73413192-c4d1-4697-a1cc-363ed2a81b0bSPL ID 73413192-c4d1-4697-a1cc-363ed2a81b0bSPL set ID 66fe5457-fe15-4e33-b47e-2c0dc9b171f6UNII VB06AV5US8, 6GLA1946WX, ZW3Z11D0JV, 398IYQ16YV, 7B69B0BD62, 6RV024OAUQ, S7V92P67HO, T7J046YI2B, 810258W28U, 993QHL78E6, 877L01IZ0P, RWG7BD1032, 0YPR65R21J, 8E272251DI, QDL83WN8C2, ETJ7Z6XBU4, 9N2N2Y55MH

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

N443857054701 followed by a unit qualifier and the quantity

Package 43857-0547-01. 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 Aug 28, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms of cough with expectoration & dyspepsia, ill effects of melons, water & dried fruits, thick yellow ropy mucous secretions.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)