NYLOXIN STAGE 2 PAIN RELIEF (NAJA NAJA VENOM) SPRAY, METERED [RECEPTOPHARM INC]

  • Home
  • NYLOXIN STAGE 2 PAIN RELIEF (NAJA NAJA VENOM) SPRAY, METERED [RECEPTOPHARM INC]

NYLOXIN STAGE 2 PAIN RELIEF (NAJA NAJA VENOM) SPRAY, METERED [RECEPTOPHARM INC]
PDF | XML
NDC 47219-203-10
Set ID 9ad47340-ddbf-11de-a1c2-0002a5d5c51b
Category HUMAN OTC DRUG LABEL
Packager RECEPTOPHARM INC
Generic Name
Product Class
Product Number
Application Number
View All Sections
  • Active Ingredients

    Asian Cobra venom 4X

  • Purpose

    Analgesic

  • Directions:

    • Break protective tab off.
    • Turn Press lock so spray nozzle is visible in front.
    • Press down on pump.
    • Spray directly into mouth or under tongue.

    Use 2 sprays 4 times a day

    Note: It may take several days to induce relief. Use within 90 days of opening.
    Store at 50° to 80°F

  • Warnings:

    For oral use only. Over use may induce headaches. Not for use by pregnant women. If symptoms persist, consult a physician.

  • SPL UNCLASSIFIED SECTION

    For more information visit
    www.Nyloxin.com

    Manufactured for: Nutra Pharma
    Plantation, FL 33313

  • PRINCIPAL DISPLAY PANEL

    Package Label - Principal Display Panel – 0.5 oz Spray Label

    0.5 oz Spray Bottle Label

  • INGREDIENTS AND APPEARANCE
    NYLOXIN  STAGE 2 PAIN RELIEF
    naja naja venom spray, metered
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47219-203
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM) NAJA NAJA VENOM.035 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    XYLITOL (UNII: VCQ006KQ1E)  
    2-(DIETHYLAMINO)ETHANOL (UNII: S6DL4M053U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47219-203-101 in 1 BOX
    115 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved homeopathic08/25/2009
    Labeler - RECEPTOPHARM INC (145377888)
    Establishment
    NameAddressID/FEIBusiness Operations
    RECEPTOPHARM INC145377888ANALYSIS, MANUFACTURE, API MANUFACTURE
    Establishment
    NameAddressID/FEIBusiness Operations
    LIQUID PACKAGING RESOURCES018935165MANUFACTURE
View All Sections

Related Drugs

Search DailyMed Drugs