Swelling HP NDC 43406-0627

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0627Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0627Add 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
43406-0627-1	43406062701	30 mL in 1 BOTTLE, DROPPER (43406-0627-1)Marketed from Jun 1, 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): Swelling HP
Generic name (nonproprietary): apis mellifera, arsenic trioxide, cinchona officinalis bark, digitalis, lachesis muta venom, lycopodium clavatum spore, sodium sulfate, toxicodendron pubescens leaf, sambucus nigra flowering top, strophanthus hispidus seed
Active ingredients: Apis mellifera — 30 [hp_C]/mLArsenic trioxide — 30 [hp_C]/mLCinchona officinalis bark — 30 [hp_C]/mLDigitalis — 30 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSodium sulfate — 30 [hp_C]/mLToxicodendron pubescens leaf — 30 [hp_C]/mLSambucus nigra flowering top — 30 [hp_C]/mLStrophanthus hispidus seed — 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 29, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43406-0627_92875cfb-2144-4616-9bbb-13cfa639f95aSPL ID 92875cfb-2144-4616-9bbb-13cfa639f95aSPL set ID 88e50673-d47a-49f8-8be9-253f8b735c4eUNII 7S82P3R43Z, S7V92P67HO, S003A158SB, F1T8QT9U8B, VSW71SS07I, C88X29Y479, 0YPR65R21J, 6IO182RP7A, CT03BSA18U, MO892VI77KUPC 0877730004598
Pharmacologic class: Standardized Insect Venom 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

N443406062701 followed by a unit qualifier and the quantity

Package 43406-0627-01. 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 19, 2022.

Indications (excerpt from the label)

USES: Temporarily relieves sensation of soreness & swelling of hands & feet.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)