Label: BASIC ESSENTIALS ASTRINGENT- salicylic acid liquid

  • NDC Code(s): 76176-353-01
  • Packager: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 1, 2020

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  • Drug Facts Active ingredient

    Salicylic Acid 0.5%

  • Purpose

    Acne treatment

  • Uses

    for the treatment of acne.

  • Warnings

    For external use only.

    Flammable, keep away from open flame.

    When using this product

    • avoid contact with eyes. If contact occurs, immediately flush with water.
    • 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 once medication should be used, unless directed by a doctor.
  • Keep out of reach of children.

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

  • Directions:

    • Wash face as you normally would and pat dry with a clean towel.
    • Apply a small amount to cotton ball or pad and apply using a dabbing motion.
    • Take care to avoid rubbing in eyes.
    • Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy.
    • Apply a light moisturizer after using astringent
    • If bothersome drying or peeling occurs, reduce application.
  • Inactive Ingredients

    Water (Aqua), Alcohol (24.5%), Propylene Glycol, Glycerin, PEG-32, Algae Extract, DMDM Hydantoin, Dimethicone Propyl PG-Betaine, Sodium Citrate, Aloe Barbadensis Leaf Extract, Benzophenone-4, Denatonium Benzoate, Fragrance, FD&C Yellow No.5

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    BASIC ESSENTIALS ASTRINGENT 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-353
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    ALCOHOL (UNII: 3K9958V90M)  
    PEG-32 DISTEARATE (UNII: 5730584SOC)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    WATER (UNII: 059QF0KO0R)  
    BENZOPHENONE (UNII: 701M4TTV9O)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-353-01236.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D09/01/2020
    Labeler - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098)
    Registrant - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098)
    Establishment
    NameAddressID/FEIBusiness Operations
    NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.530766098manufacture(76176-353)
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