Label: CROMOLYN SODIUM spray, metered

  • NDC Code(s): 57782-397-26
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 1, 2021

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  • SPL UNCLASSIFIED SECTION
    (Adults and children 2 years and older)
  • Active ingredient (per spray)
    Cromolyn sodium 5.2 mg
  • Purpose
    Nasal allergy symptom controller
  • Uses
    to prevent and relieve nasal symptoms of hay fever and other nasal allergies: • runny/itchy nose - • sneezing - • allergic stuffy nose
  • Warnings
    For external use only - Do not use - • if you are allergic to any of the ingredients - Ask a doctor before use if you have - • fever - • discolored nasal discharge - • sinus ...
  • Directions
    • see package insert on how to use pump - • parent or care provider must supervise the use of this product by young children - • adults and children 2 years and older: • spray once into each ...
  • Other information
    • store between 20-25°C (68-77°F) • protect from light - • keep carton and package insert. They contain important instructions. • see bottom panel for lot number and expiration date
  • Inactive ingredients
    benzalkonium chloride, edetate disodium, purified water
  • Questions or comments?
    Call toll-free 1-800-323-0000
  • Package/Label Principal Display Panel
    HealthGuard - NDC 57782-397-26 - Cromolyn - Sodium Nasal - Solution, USP - NASAL SPRAY - Nasal Allergy Symptom Controller - For intranasal use only. Prevents and Relieves - Nasal Allergy ...
  • INGREDIENTS AND APPEARANCE
    Product Information