Label: SALINE WIPES- sodium chloride cloth

  • NDC Code(s): 77267-007-01
  • Packager: Ningbo Riway Industrial Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated November 21, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient(s)

    Sodium chloride .90%

  • Purpose

    Nasal Decongestant

  • Use

    For nasal decongestant and gentle cleansing of the nose and facial areas.

  • Warnings

    For external use only.

  • Do not use

    If you are allergic to any of the ingredients.

  • WHEN USING

    When using this product,avoid contact with eyes and mouth. If product gets in the eyes,flush thoroughly with water.

  • STOP USE

    Discontinue use and contact a doctor if irritation and redness develop and condition persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Remove wipe and unfold.

    Gently wipe the nose and face.

    Throw used wipe in trash. Do not flush.

  • Inactive ingredients

    Purified Water, Aloe Barbadensis Leaf Extract.

  • Package Label - Principal Display Panel

    SALINE WIPES PACKAGING FINAL 3

  • INGREDIENTS AND APPEARANCE
    SALINE WIPES 
    sodium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77267-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE0.9 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77267-007-01259.2 mL in 1 BAG; Type 0: Not a Combination Product10/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/17/2020
    Labeler - Ningbo Riway Industrial Co., Ltd. (540997562)
    Registrant - Ningbo Riway Industrial Co., Ltd. (540997562)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Riway Industrial Co., Ltd.540997562manufacture(77267-007)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!