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
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INGREDIENTS AND APPEARANCE
GINGI-AID SOLUTION
aluminum chloride 25% solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10129-017 Route of Administration DENTAL, ORAL, PERIODONTAL, SUBGINGIVAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE 3.75 g in 15 mL Inactive Ingredients Ingredient Name Strength CHLOROBUTANOL (UNII: HM4YQM8WRC) 3 mg in 15 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10129-017-02 15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/04/1990 2 NDC:10129-017-03 40 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/04/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 04/04/1990 Labeler - Gingi-Pak a Division of the Belport (008480121)