Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Candida NDC 81825-0004
Baptisia tinctoria whole 4 [hp_X]/mL + 15 more ingredients · Liquid · Oral · Zorex International
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 81825-0004-1 | 8182500040181825000401 | 30 mL in 1 BOTTLE, DROPPER (81825-0004-1)Marketed from Dec 22, 2021 |
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
- Generic name (nonproprietary)
- baptisia tinctoria, echinacea purp, glycyrrhiza glabra, astragalus, candida alb, borax, calc carb, kreosotum, lycopodium, nux vom, phosphoricum ac, pulsatilla, sepia, thuja occ, nat phos, nitricum ac
- Active ingredients
- Baptisia tinctoria whole — 4 [hp_X]/mLEchinacea purpurea whole — 4 [hp_X]/mLGlycyrrhiza glabra — 4 [hp_X]/mLAstragalus nuttallii leaf — 6 [hp_X]/mLCandida albicans — 200 [hp_C]/mLSodium borate — 30 [hp_C]/mLOyster shell calcium carbonate, Crude — 30 [hp_C]/mLWood creosote — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphoric acid — 30 [hp_C]/mLPulsatilla vulgaris whole — 30 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mLThuja occidentalis leafy twig — 30 [hp_C]/mLSodium phosphate, Dibasic, Heptahydrate — 30 [hp_C]/mLNitric acid — 30 [hp_C]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Zorex InternationalNDC labeler code 81825
- 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 81825-0004_32b5e01c-67ef-4251-b6a4-b7e007fafc83SPL ID 32b5e01c-67ef-4251-b6a4-b7e007fafc83SPL set ID c6595326-6d04-499e-9eb7-0a4cd2ba48fdUNII 5K1UO2888Y, QI7G114Y98, 2788Z9758H, NC1P15G4KZ, 4D7G21HDBC, 91MBZ8H3QO, 2E32821G6I, 3JYG22FD73, C88X29Y479, 269XH13919, E4GA8884NN, I76KB35JEV, QDL83WN8C2, 1NT28V9397, 70WT22SF4B, 411VRN1TV4UPC 0713289148102
- 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
N481825000401followed by a unit qualifier and the quantityPackage 81825-0004-01. 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.**
Excerpt only. Read the full label for complete information.
About NDC 81825-0004
- What is NDC 81825-0004?
- 81825-0004 is the product NDC for Candida, Baptisia tinctoria whole 4 [hp_X]/mL + 15 more ingredients liquid, listed with the FDA by Zorex International. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Candida (Baptisia Tinctoria, Echinacea Purp, Glycyrrhiza Glabra, Astragalus, Candida Alb, Borax, Calc Carb, Kreosotum, Lycopodium, Nux Vom, Phosphoricum Ac, Pulsatilla, Sepia, Thuja Occ, Nat Phos, Nitricum Ac).
- What is the active ingredient?
- Baptisia tinctoria whole, Echinacea purpurea whole, 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, Pulsatilla vulgaris whole, Sepia officinalis juice, Thuja occidentalis leafy twig, Sodium phosphate, Dibasic, Heptahydrate, Nitric acid.
- Who is the labeler?
- Zorex International, NDC labeler code 81825. 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?
- 2 other product NDCs are listed under this name. See all Candida NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Candida products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Candidacandida albicans | Candida albicans 12 [hp_X]/mL | LiquidOral | BioActive Nutritional, Inc. | 43857-0177 | 43857-0177-01 |
| Candidacandida albicans | Candida albicans .05 g/mL | InjectionCutaneous, Intradermal, Subcutaneous | Allermed Laboratories, Inc. | 49643-105 | 49643-0105-0549643-0105-1049643-0105-30+1 more |