What is NDC 63479-0203?

63479-0203 is the product NDC for B03 Sinus Relief, Lactose, Unspecified form 12 [hp_X]/mL + 18 more ingredients solution/ drops, listed with the FDA by Apex Energetics Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

B03 Sinus Relief (Allium cepa, Calcarea iodata, Calcarea sulphurica, Echinacea angustifolia, Echinacea purpurea, Euphorbium officinarum, Hepar sulphuris calcareum, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Kali muriaticum, Kali sulphuricum, Lac defloratum, Luffa operculata, Mercurius sulphuratus ruber, Phosphorus, Pulsatilla vulgaris, Saccharum lactis, Thuja occidentalis).

What is the active ingredient?

Lactose, Unspecified form, Thuja occidentalis leafy twig, Potassium sulfate, Goldenseal, Potassium dichromate, Potassium chloride, Pulsatilla vulgaris, Phosphorus, Skim milk, Calcium iodide, Echinacea angustifolia, Echinacea purpurea, Euphorbia resinifera resin, Calcium sulfide, Histamine dihydrochloride, Mercuric sulfide, Onion, Calcium sulfate anhydrous, Luffa operculata fruit.

Apex Energetics Inc., NDC labeler code 63479. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for B03 Sinus Relief?

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.

B03 Sinus Relief NDC 63479-0203 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0203Add 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
63479-0203-1	6347902030163479020301	30 mL in 1 BOTTLE, GLASS (63479-0203-1)Marketed from Feb 15, 1995

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): B03 Sinus ReliefSuffix: Sinus Relief
Generic name (nonproprietary): allium cepa, calcarea iodata, calcarea sulphurica, echinacea angustifolia, echinacea purpurea, euphorbium officinarum, hepar sulphuris calcareum, histaminum hydrochloricum, hydrastis canadensis, kali bichromicum, kali muriaticum, kali sulphuricum, lac defloratum, luffa operculata, mercurius sulphuratus ruber, phosphorus, pulsatilla vulgaris, saccharum lactis, thuja occidentalis
Active ingredients: Lactose, Unspecified form — 12 [hp_X]/mLThuja occidentalis leafy twig — 10 [hp_X]/mLPotassium sulfate — 12 [hp_X]/mLGoldenseal — 1 [hp_X]/mLPotassium dichromate — 15 [hp_X]/mLPotassium chloride — 10 [hp_X]/mLPulsatilla vulgaris — 12 [hp_X]/mLPhosphorus — 8 [hp_X]/mLSkim milk — 30 [hp_X]/mLCalcium iodide — 12 [hp_X]/mLEchinacea angustifolia — 1 [hp_X]/mLEchinacea purpurea — 1 [hp_X]/mLEuphorbia resinifera resin — 6 [hp_X]/mLCalcium sulfide — 15 [hp_X]/mLHistamine dihydrochloride — 30 [hp_X]/mLMercuric sulfide — 12 [hp_X]/mLOnion — 12 [hp_X]/mLCalcium sulfate anhydrous — 12 [hp_X]/mLLuffa operculata fruit — 12 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.NDC labeler code 63479
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 15, 1995
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Calcium (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 63479-0203_47428a99-4994-566c-e063-6294a90a939bSPL ID 47428a99-4994-566c-e063-6294a90a939bSPL set ID bad83f77-e9ae-7118-e053-2a95a90aa737UNII J2B2A4N98G, 1NT28V9397, 1K573LC5TV, ZW3Z11D0JV, T4423S18FM, 660YQ98I10, I76KB35JEV, 27YLU75U4W, 6A001Y4M5A, 8EKI9QEE2H, VB06AV5US8, QI7G114Y98, 1TI1O9028K, 1MBW07J51Q, 3POA0Q644U, ZI0T668SF1, 492225Q21H, E934B3V59H, C4MO6809HUUPC 0818960010188
Pharmacologic class: Blood Coagulation Factor; Non-Standardized Food Allergenic Extract; Osmotic Laxative; Phosphate Binder; Potassium Salt

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

NDC on a medical claim

N463479020301 followed by a unit qualifier and the quantity

Package 63479-0203-01. 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 31, 2025.

Indications (excerpt from the label)

Uses: For temporary relief of minor: sinus congestion* coughing* fatigue* nasal discharge* frontal headache* muscle aches* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63479-0203

What is NDC 63479-0203?: 63479-0203 is the product NDC for B03 Sinus Relief, Lactose, Unspecified form 12 [hp_X]/mL + 18 more ingredients solution/ drops, listed with the FDA by Apex Energetics Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: B03 Sinus Relief (Allium cepa, Calcarea iodata, Calcarea sulphurica, Echinacea angustifolia, Echinacea purpurea, Euphorbium officinarum, Hepar sulphuris calcareum, Histaminum hydrochloricum, Hydrastis canadensis, Kali bichromicum, Kali muriaticum, Kali sulphuricum, Lac defloratum, Luffa operculata, Mercurius sulphuratus ruber, Phosphorus, Pulsatilla vulgaris, Saccharum lactis, Thuja occidentalis).
What is the active ingredient?: Lactose, Unspecified form, Thuja occidentalis leafy twig, Potassium sulfate, Goldenseal, Potassium dichromate, Potassium chloride, Pulsatilla vulgaris, Phosphorus, Skim milk, Calcium iodide, Echinacea angustifolia, Echinacea purpurea, Euphorbia resinifera resin, Calcium sulfide, Histamine dihydrochloride, Mercuric sulfide, Onion, Calcium sulfate anhydrous, Luffa operculata fruit.
Who is the labeler?: Apex Energetics Inc., NDC labeler code 63479. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for B03 Sinus Relief?: 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.