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 NDC11-digit (billing)PackageCopy
43406-0672-1434060672014340606720130 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.NDC labeler code 43406
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

USES: Temporarily relieves symptoms associated with vaginal yeast infection.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43406-0672

What is NDC 43406-0672?
43406-0672 is the product NDC for Candida HP, Baptisia tinctoria root 4 [hp_X]/mL + 15 more ingredients liquid, listed with the FDA by Natural Creations, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Candida HP (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).
What is the active ingredient?
Baptisia tinctoria root, Echinacea purpurea, Glycyrrhiza glabra, Astragalus nuttallii leaf, Sodium borate, Oyster shell calcium carbonate, Crude, Wood creosote, Lycopodium clavatum spore, Sodium phosphate, Dibasic, Heptahydrate, Nitric acid, Strychnos nux-vomica seed, Phosphoric acid, Pulsatilla vulgaris, Sepia officinalis juice, Thuja occidentalis leafy twig, Candida albicans.
Who is the labeler?
Natural Creations, Inc., NDC labeler code 43406. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Candida HP?
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.

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