XS GUARD- sanitizer liquid XS CLEAN- hand sanitizer gel XS GUARD- handwipe liquid
XS Guard by
Drug Labeling and Warnings
XS Guard by is a Otc medication manufactured, distributed, or labeled by XS Supply LLC. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- use as needed
- Warning - Keep out of the reach of children
- inactive ingredients
- indications for use
- keep out of the reach of children
- active ingredient Isoproanol and active ingredient ethanol
- Purpose is hand sanitization
- Package Labels Display Panel
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INGREDIENTS AND APPEARANCE
XS GUARD
sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 80015-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 30 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 80015-112-01 1 mL in 1 CANISTER; Type 0: Not a Combination Product 08/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/11/2020 XS CLEAN
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 80015-223 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 30 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 80015-223-01 1 mL in 1 CANISTER; Type 0: Not a Combination Product 08/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/11/2020 08/27/2021 XS GUARD
handwipe liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 80015-333 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 30 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 80015-333-01 10 mL in 1 CONTAINER; Type 0: Not a Combination Product 08/11/2020 08/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/11/2020 08/27/2021 Labeler - XS Supply LLC (080284229)
see attached label copies
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