Label: EUNOS ADVANCED HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75007-001-01, 75007-001-02, 75007-001-03 - Packager: YIRONG TRADING (NANJING) CO., LTD
- 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 April 26, 2020
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- Active Ingredient
- Purpose
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- Directions
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
EUNOS ADVANCED HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75007-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75007-001-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2020 2 NDC:75007-001-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2020 3 NDC:75007-001-03 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/09/2020 Labeler - YIRONG TRADING (NANJING) CO., LTD (554529568)