17089-420 : Micox Oral Solution/ Drops


NDC: 17089-420
Labeler: Guna Spa
Product Type: Human OTC Drug
Drug Name: Micox
Dosage Form: Oral Solution/ Drops
Rev. Date: 


NDC Package Codes:

  • 17089-420-18: 1 BOTTLE, DROPPER IN 1 BOX (17089‑420‑18) > 30 ML IN 1 BOTTLE, DROPPER

Active Ingredients:

  • Aspergillus Niger Var. Niger
  • Candida Albicans
  • Malic Acid
  • Centella Asiatica
  • Mercuric Chloride
  • Rhizopus Stolonifer
  • Sodium Diethyl Oxalacetate
  • Tabebuia Impetiginosa Bark
  • Sulfur

Dosage Strength:

  • 30 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 12 [hp_X]/30mL
  • 6 [hp_X]/30mL
  • 6 [hp_X]/30mL
  • 30 [hp_X]/30mL
  • 12 [hp_X]/30mL
  • 4 [hp_X]/30mL
  • 6 [hp_X]/30mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Fungal Proteins [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Fungal Allergenic Extract [EPC]

NDC QR Code

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NDC 17089-420 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.