Respirasode NDC 43406-0089

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0089Add 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
43406-0089-1	43406008901	30 mL in 1 BOTTLE, DROPPER (43406-0089-1)Marketed from May 22, 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): Respirasode
Generic name (nonproprietary): bryonia, dulcamara, kali carb, sanguinaria, belladonna, bromium, candida alb, candida parap, conium, lycopodium, pulsatilla, secale, silicea, sticta, sulphur, ustilago maidis
Active ingredients: Bryonia alba root — 30 [hp_C]/mLSolanum dulcamara top — 30 [hp_C]/mLPotassium carbonate — 30 [hp_C]/mLSanguinaria canadensis root — 30 [hp_C]/mLAtropa belladonna — 30 [hp_C]/mLBromine — 30 [hp_C]/mLCandida albicans — 30 [hp_C]/mLCandida parapsilosis — 30 [hp_C]/mLConium maculatum flowering top — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLPulsatilla vulgaris whole — 30 [hp_C]/mLClaviceps purpurea sclerotium — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLLobaria pulmonaria — 30 [hp_C]/mLSulfur — 30 [hp_C]/mLUstilago maydis — 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: May 22, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43406-0089_d21ac507-d019-40f1-b788-c4be6b8deeedSPL ID d21ac507-d019-40f1-b788-c4be6b8deeedSPL set ID ce06327f-7e5e-420a-9b61-0d410f9e10d6UNII T7J046YI2B, KPS1B1162N, BQN1B9B9HA, N9288CD508, WQZ3G9PF0H, SBV4XY874G, 4D7G21HDBC, 0KZ676D44N, Q28R5GF371, C88X29Y479, I76KB35JEV, 01G9XEA93N, ETJ7Z6XBU4, D1YM0P5Z2T, 70FD1KFU70, 4K7Z7K7SWGUPC 0877730002594
Pharmacologic class: Non-Standardized Fungal 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

N443406008901 followed by a unit qualifier and the quantity

Package 43406-0089-01. 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 16, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves cough, stuffy and dry nose, and/or symptoms related to cold.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)