Label: SUNTAN- suntan lotion cream, augmented

  • NDC Code(s): 85421-001-00
  • Packager: Guangzhou shangwei Beauty TechnologyCo.,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 March 22, 2025

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  • OTC-ACTIVE INGREDIENT SECTION
    OTC-ACTIVE INGREDIENT SECTION:Water,
  • OTC-PURPOSR SECTION
    OTC - PURPOSE SECTION
  • OTC-KEEP OUT OF REACH OF CHILDREN SECTION
    OTC-KEEP OUT OF REACH OF CHILDREN SECTION:To avoid danger of suffocation keep this bag away from babies and children Do not use this bag in cribs,beds carriages or play pens.this bag is not a ...
  • INDICATIONS
    1.For external use only,Avoid contact with eyes. 2.Keep away from babies and children. 3.If feel any discomfort after use，please stop using it - 4.Keep away from fire sources and direct ...
  • WARNINGS SECTION
    To avoid danger of suffocation keep this bag away from babies and children.Do not use this bag in cribs beds,besd,cariages,or play pens.this bag is not a toy.
  • DOSAGE
    ERROR HAS OCCURRED 1g
  • INACTIVE INGREDIENT
    INACTIVE INGREDIENT SECTION :Oryza Sativa (Rice),Dibutyl Adipate,Propanediol,Diethylamino Hydroxybenzoyl Hexyl Benzoate,Polymethylsilsesquioxane,Ethylhexyl Triazone,Niacinamide,Methylene ...
  • PRINCIPAL DISPLAY PANEL
    2
  • INGREDIENTS AND APPEARANCE
    Product Information
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