Label: THAYERS SINCE 1847 NATURAL REMEDIES BLEMISH CLEARING WITCH HAZEL ALOE VERA FORMULA CLEANSER- salicylic acid gel

  • NDC Code(s): 49967-051-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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

View All Sections
  • Active ingredient


    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Uses

    • for the treatment of acne
    • clears acne blemishes and allows skin to heal
    • helps prevent the development of new acne blemishes

  • Warnings

    For external use only

  • When using this product

    skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. 

  • Keep out of reach of children.

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

  • Directions

    • wet the skin
    • dispense into wet hands and massage area gently
    • rinse thoroughly with warm water
    • cleanse twice daily
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

  • Other information

    store at 15°-30° C (59°-86° F) away from direct sunlight

  • Inactive ingredients

    water, natural beatine, glycerin, lauryl glucoside, sodium cocoyl isethionate, decyl glucoside, hamamelis virginiana (witch hazel) bark/leaf/twig extract, aloe barbadensis leaf extract, phenoxyethanol, ethylhexylglycerin, cymbopogon schoenanthus (lemongrass) leaf extract blend, melaleuca
    alternafolia (tea tree) leaf oil, hydroxypropyl methylcellulose, guar cydroxypropyltrimonium chloride

  • PRINCIPAL DISPLAY PANEL

    image of a label

    image of a label
  • INGREDIENTS AND APPEARANCE
    THAYERS SINCE 1847 NATURAL REMEDIES BLEMISH CLEARING WITCH HAZEL ALOE VERA FORMULA CLEANSER 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-051-01118 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00601/01/2022
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    Continental Manufacturing Chemist081171390manufacture(49967-051)
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!