Label: DRS. ACNE CLEAR- salicylic acid gel

  • NDC Code(s): 80489-300-01, 80489-300-02
  • Packager: OL PHARMA TECH, LLC Drs. PHARMACY
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 8, 2023

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

View All Sections
  • ACTIVE INGREDIENT

    Salicylic Acid 0.5% w/w.

  • PURPOSE

    Acne treatment

  • USES

    For the treatment of acne. Dries and clears acne pimples, blackheads and whiteheads and allows skin to heal.

  • DO NOT USE

    if you have sensitive skin or are sensitive to salicylic acid

  • DIRECTIONS

    Morning and evening, after a thorough cleansing of the skin, apply acne clear gel locally on cutanous imperfections. Then apply the usual day or night cream. Renew application 1 to 3 times daily.

  • WARNINGS

    For external use only. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Avoid direct contact with the eyes. If product gets into the eyes, rinse liberally with water. Discontinue use if skin irritation develops or increases. If irritation persists, consult a doctor.

  • WHEN USING THIS PRODUCT

    Avoid contact with eyes, lips, and mouth.

  • KEEP OUT OF REACH OF CHILDREN

    if swallowed, get medical help or contact poison control center right away

  • INACTIVE INGREDIENT

    carbomer interpolymer type A, trolamine, vitamin E, propylene glycol, water, isopropyl alcohol, methyl paraben, EDTA, propyl paraben, DMDM hydantoin

  • OTHER INFORMATION

    • store at 15-30 C ( 59-86 F)
    • close cap tightly after use
    • keep away from heat
  • QUESTIONS

    www.drspharmacyusa.com

  • PACKAGE LABEL

    acne clear

  • INGREDIENTS AND APPEARANCE
    DRS. ACNE CLEAR 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-300
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80489-300-011 in 1 CARTON02/01/2022
    120 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
    2NDC:80489-300-021 in 1 CARTON02/01/2022
    230 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00602/01/2022
    Labeler - OL PHARMA TECH, LLC Drs. PHARMACY (021170377)
    Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
    Establishment
    NameAddressID/FEIBusiness Operations
    OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-300)
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!