17312-002 : Blur Relief Intraocular Liquid


NDC: 17312-002
Labeler: Trp Company
Product Type: Human OTC Drug
Drug Name: Blur Relief
Dosage Form: Intraocular Liquid
Rev. Date: 


NDC Package Codes:

  • 17312-002-11: 1 BOTTLE, DROPPER IN 1 PACKAGE (17312‑002‑11) > 15 ML IN 1 BOTTLE, DROPPER

Active Ingredients:

  • Jacobaea Maritima
  • Calcium Fluoride
  • Conium Maculatum Flowering Top
  • Euphrasia Stricta
  • Gelsemium Sempervirens Root
  • Sodium Chloride
  • Ruta Graveolens Flowering Top

Dosage Strength:

  • 5 [hp_X]/mL
  • 13 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL
  • 6 [hp_X]/mL

Pharmaceutical Classes:

  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]

NDC QR Code

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NDC 17312-002 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.