Label: NATURAL SAVON 4IN1 PLUS- glycerin cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 March 21, 2017

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients: GLYCERIN 4.3%

  • INACTIVE INGREDIENT

    Inactive ingredients: AQUA (WATER), SODIUM LAURETH SULFATE, COCO-GLUCOSIDE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER CAPRYLIC/CAPRIC TRIGLYCERIDE, GALACTOARABINAN, ILLITE, BENZYL ALCOHOL, COCAMIDOPROPYL BETAINE, PARFUM (FRAGRANCE), SODIUM BENZOATE, HYDROXYPROPYL GUAR, XANTHAN GUM, CITRIC ACID, POTASSIUM SORBATE, DEHYDROACETIC ACID, BENZOIC ACID, SODIUM HYDROXIDE, ALGAE EXTRACT, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN

  • PURPOSE

    Purpose: Remove impurities and makeup

  • WARNINGS

    Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications & Usage: Use once or twice daily

  • DOSAGE & ADMINISTRATION

    Dosage & Administration: Place small amount into palm, add water, then massage into the face. Rinse thoroughly.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NATURAL SAVON 4IN1 PLUS 
    glycerin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71276-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN8.6 g  in 200 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71276-020-021 in 1 CARTON03/02/2017
    1NDC:71276-020-01200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/02/2017
    Labeler - ULAB (688976692)
    Registrant - ULAB (688976692)
    Establishment
    NameAddressID/FEIBusiness Operations
    ULAB688976692relabel(71276-020)
    Establishment
    NameAddressID/FEIBusiness Operations
    U-LAB Switzerland AG485958743manufacture(71276-020)
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!