Label: EEZYSUN AFTER SUN COOLING- aniba rossadora,calendula officinalis,lavandula officialls,matricaria chamomilla,mentha piperita,sodium hyaluronate cream

  • NDC Code(s): 70116-025-01
  • Packager: BIO EARTH MANUFACTURING (PTY) LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated May 28, 2025

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

  • Drug Facts

  • Active ingredients

    Aniba Rossadora 0.35 %
    Calendula Officinalis 0.95 %
    Lavandula Officialls 0.75 %
    Matricaria Chamomilla 0.6 %
    Mentha Piperita 0.8 %
    Sodium Hyaluronate 0.1 %

  • Purpose

    Relaxing, cooling, anti-inflammatory, soothing, relieving

  • Uses

    Cooling down the skin

  • Warnings

    For external use only.

    • Not suitable for epileptics
    • Not suitable for people with uncontrolled hyper-tension. 
    • Not recommended during pregnancy and lactation
    • Not suitable for individuals with known sensitivity to any of the ingredients. 
    • Avoid contact with eyes.
  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Shake well before use

    Adults: Apply up to three times per day as needed

    Children: Use conservatively for children younger than two years

  • Inactive ingredients

    Aloe Vera, Aqua, Carbomer, Ethylhexlglycerin, Glycerin, Phenoxyethanol, Sodium Hydroxide

  • Other information

    Store at or below 77⁰ F/25⁰C

    Do not use if seal is broken.

    product the product in this container from excessive heat and direact sun

  • Product label

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  • INGREDIENTS AND APPEARANCE
    EEZYSUN AFTER SUN COOLING 
    aniba rossadora,calendula officinalis,lavandula officialls,matricaria chamomilla,mentha piperita,sodium hyaluronate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70116-025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BRAZILIAN ROSEWOOD OIL (UNII: F2522O5L7B) (BRAZILIAN ROSEWOOD OIL - UNII:F2522O5L7B) BRAZILIAN ROSEWOOD OIL0.35 g  in 100 mL
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP0.95 g  in 100 mL
    LAVENDER OIL (UNII: ZBP1YXW0H8) (ENGLISH LAVENDER OIL - UNII:ZBP1YXW0H8) LAVENDER OIL0.75 g  in 100 mL
    MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ) (MATRICARIA CHAMOMILLA - UNII:G0R4UBI2ZZ) MATRICARIA CHAMOMILLA WHOLE0.6 g  in 100 mL
    PEPPERMINT OIL (UNII: AV092KU4JH) (PEPPERMINT - UNII:V95R5KMY2B) PEPPERMINT OIL0.8 g  in 100 mL
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70116-025-011 in 1 CARTON05/23/2025
    1100 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/23/2025
    Labeler - BIO EARTH MANUFACTURING (PTY) LTD (639768436)