Label: ALMA RITUAL HERBAL- hand sanitizer spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 10, 2022

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient

    Alcohol 70% v/v Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Uses

    • Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
  • Warnings

    For external use only

    Flammable. Keep away from heat and flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • When using this product

    Keep out of eyes, ears and, mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    if irritation or rash occurs. These may be signs of a serious condition.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry
    • Supervise children under 6 years of age when using this product to avoid swallowing
  • Other information:

    • Store between 15-35 C (59-95 F)
    • Avoid freezing and excessive heat above 40 C (104 F)
  • Inactive Ingredients:

    Citrus Aurantium Dulcis Peel Oil, Eucalyptus Globulus Leaf Oil, Glycerin, Lavandula Hybrida Oil, Mentha Pipperita (Peppermint) Oil, Rosmarinus Officinalis (Rosemary) Extract, Water

  • P.D.P.

    100 mL NDCc: 82933-100-01

  • INGREDIENTS AND APPEARANCE
    ALMA RITUAL HERBAL 
    hand sanitizer spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82933-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MENTHA PIPERITA (UNII: 79M2M2UDA9)  
    WATER (UNII: 059QF0KO0R)  
    CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82933-100-01100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/11/2022
    Labeler - Artieda Lozada Johanna Elizabeth (813545114)
    Registrant - AY CONSULTING SERVICES, LLC (078311971)
    Establishment
    NameAddressID/FEIBusiness Operations
    Arteida Lozada Johanna Elizabeth813545114manufacture(82933-100)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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