Candida HP NDC 43406-0672

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0672Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0672Add 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
43406-0672-1	43406067201	30 mL in 1 BOTTLE, DROPPER (43406-0672-1)Marketed from Jan 1, 2018

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): Candida HP
Generic name (nonproprietary): baptisia tinctoria root, echinacea purpurea, glycyrrhiza glabra, astragalus nuttallii leaf, candida albicans, sodium borate, oyster shell calcium carbonate, crude, wood creosote, lycopodium clavatum spore, strychnos nux-vomica seed, phosphoric acid, anemone pulsatilla, sepia officinalis juice, thuja occidentalis leafy twig, sodium phosphate, dibasic, heptahydrate, nitric acid
Active ingredients: Baptisia tinctoria root — 4 [hp_X]/mLEchinacea purpurea — 4 [hp_X]/mLGlycyrrhiza glabra — 4 [hp_X]/mLAstragalus nuttallii leaf — 6 [hp_X]/mLSodium borate — 30 [hp_C]/mLOyster shell calcium carbonate, Crude — 30 [hp_C]/mLWood creosote — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSodium phosphate, Dibasic, Heptahydrate — 30 [hp_C]/mLNitric acid — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphoric acid — 30 [hp_C]/mLPulsatilla vulgaris — 30 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mLThuja occidentalis leafy twig — 30 [hp_C]/mLCandida albicans — 200 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43406-0672_0bc1674e-2c7f-4d3f-808c-e96619c55d03SPL ID 0bc1674e-2c7f-4d3f-808c-e96619c55d03SPL set ID b587a3f0-628b-41f7-8afb-2cdcd896279eUNII 5EF0HWI5WU, QI7G114Y98, 2788Z9758H, NC1P15G4KZ, 91MBZ8H3QO, 2E32821G6I, 3JYG22FD73, C88X29Y479, 70WT22SF4B, 411VRN1TV4, 269XH13919, E4GA8884NN, I76KB35JEV, QDL83WN8C2, 1NT28V9397, 4D7G21HDBCUPC 0877730000743
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant 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

N443406067201 followed by a unit qualifier and the quantity

Package 43406-0672-01. 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

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