Label: GINGI-AID SOLUTION- aluminum chloride 25% solution

  • NDC Code(s): 10129-017-02, 10129-017-03
  • Packager: Gingi-Pak a Division of the Belport
  • 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 July 20, 2022

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  • Active ingredient

    Active ingredient

  • Warnings

    Warnings

  • Precautions

    Precaution

  • Purpose

    Purpose

  • Storage

    Storage

  • Uses

    Uses

  • Contraindications

    Contraindications

  • Keep out of reach of children

    Keep out of reach of children

  • Direction

    Direction

  • Inactive ingredients

    Inactive ingredients

  • Principal display

    Principal Display-GingiAid 15ml

    Principal Display-GingiAid 40 ml

  • INGREDIENTS AND APPEARANCE
    GINGI-AID SOLUTION 
    aluminum chloride 25% solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10129-017
    Route of AdministrationDENTAL, ORAL, PERIODONTAL, SUBGINGIVAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE3.75 g  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    CHLOROBUTANOL (UNII: HM4YQM8WRC) 3 mg  in 15 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10129-017-0215 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/04/1990
    2NDC:10129-017-0340 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/04/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35004/04/1990
    Labeler - Gingi-Pak a Division of the Belport (008480121)