Inflammation II NDC 43857-0418

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0418Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0418Add 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
43857-0418-1	43857041801	30 mL in 1 BOTTLE, DROPPER (43857-0418-1)Marketed from Oct 4, 2016

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): Inflammation II
Generic name (nonproprietary): astragalus membranaceus, echinacea (angustifolia), sarsaparilla (smilax regelii), tabebuia impetiginosa, hydrastis canadensis, thyroidinum (suis), aurum metallicum, carbo animalis, causticum, gelsemium sempervirens, natrum sulphuricum, phosphorus, sulphur, thuja occidentalis
Active ingredients: Astragalus propinquus root — 3 [hp_X]/mLEchinacea angustifolia — 3 [hp_X]/mLSarsaparilla — 3 [hp_X]/mLTabebuia impetiginosa bark — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSus scrofa thyroid — 8 [hp_X]/mLGold — 12 [hp_X]/mLActivated charcoal — 12 [hp_X]/mLCausticum — 12 [hp_X]/mLGelsemium sempervirens root — 30 [hp_X]/mLSodium sulfate — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLSulfur — 30 [hp_X]/mLThuja occidentalis leafy twig — 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: Oct 4, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 43857-0418_00a77fb6-d971-4b37-8d0b-eb11407d7a79SPL ID 00a77fb6-d971-4b37-8d0b-eb11407d7a79SPL set ID 4c36e714-f564-41d3-a6b8-60e633defaffUNII 922OP8YUPF, VB06AV5US8, 2H1576D5WG, 6GLA1946WX, ZW3Z11D0JV, 6RV024OAUQ, 79Y1949PYO, 2P3VWU3H10, DD5FO1WKFU, 639KR60Q1Q, 0YPR65R21J, 27YLU75U4W, 70FD1KFU70, 1NT28V9397
Pharmacologic class: 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443857041801 followed by a unit qualifier and the quantity

Package 43857-0418-01. 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 Oct 4, 2016.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of chills up and down back; extremities heavy, ache at night; general exhaustion; dry, hard cough with weakness in the chest.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)