Label: TINCTURE GREEN- 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 January 17, 2022

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol, 30%

  • KEEP OUT OF REACH OF CHILDREN

    Warnings: Avoid contact with eyes or mucous membranes. Keep out of reach of children. Toxic by ingestion. Cannot be made nontoxic. In case of ingestion contact a poison control center.

  • INDICATIONS & USAGE

    Uses: Intended for cleaning and mild antisepsis of skin.

  • WARNINGS

    Warnings: Avoid contact with eyes or mucous membranes. Keep out of reach of children. Toxic by ingestion. Cannot be made nontoxic. In case of ingestion contact a poison control center.

  • DOSAGE & ADMINISTRATION

    Directions: Mix with water. Lather and rinse.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water

  • PURPOSE

    Purpose: Antiseptic

  • greensoaplabel.jpg

    greensoaplabel.jpg

  • INGREDIENTS AND APPEARANCE
    TINCTURE GREEN 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-041
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL30 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAVENDER OIL (UNII: ZBP1YXW0H8) 0.225 g  in 100 mL
    OLEIC ACID (UNII: 2UMI9U37CP) 1.3 g  in 100 mL
    TALL OIL (UNII: 1GX6Z36A79) 24.7 g  in 100 mL
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) 10.13 g  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 4.052 g  in 100 mL
    WATER (UNII: 059QF0KO0R) 30.08 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12745-041-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    2NDC:12745-041-02473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    3NDC:12745-041-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    4NDC:12745-041-0418927 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    5NDC:12745-041-05208198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/15/1954
    Labeler - Medical Chemical Corporation (008496861)
    Registrant - Medical Chemical Corporation (008496861)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Chemical Corporation008496861manufacture(12745-041)
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!