Label: STRAIGHT SHOT- isopropyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 November 5, 2020

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

  • Active Ingredients

    Isopropyl alcohol 99% v/v.

  • Purpose

    Antiseptic

  • Uses

    Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame
    Do not use
    ■ in children less than 2 months of age
    ■ on open skin wounds.

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes,rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    ■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
    ■ Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    ■ Store between 15-30°C (59-86°F).
    ■ Avoid freezing and excessive heat above 40°C (104°F).

  • Inactive Ingredient

    water

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    STRAIGHT SHOT 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79170-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL99 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79170-002-013785 mL in 1 PACKAGE; Type 0: Not a Combination Product11/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/05/2020
    Labeler - Shift Packaging, LLC (117559082)