Label: KATE NATURALS ADVANCED HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75498-070-01, 75498-070-08, 75498-070-16 - Packager: THE DOJO LLC
- 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 15, 2020
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- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KATE NATURALS ADVANCED HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75498-070 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER 940 (UNII: 4Q93RCW27E) WATER (UNII: 059QF0KO0R) DIMETHICONE 100 (UNII: RO266O364U) FENOPROP TRIISOPROPANOLAMINE (UNII: 24FMI726KO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75498-070-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/16/2020 2 NDC:75498-070-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/16/2020 3 NDC:75498-070-01 3785 mL in 1 JUG; Type 0: Not a Combination Product 04/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/16/2020 Labeler - THE DOJO LLC (030972745) Establishment Name Address ID/FEI Business Operations THE DOJO LLC 030972745 manufacture(75498-070)