Label: HAND SANITIZER WITH ALOE EVORA LABS- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 77375-001-01, 77375-001-03 - Packager: Evora Worldwide
- 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 January 13, 2022
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- Active ingredient Purpose
- PURPOSE
- Warnings For extamaf use only. Flammable. Keep away from fire or flame.
- Keep out of reach of children.
- Uses
- Directions
- Other infonnation
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER WITH ALOE EVORA LABS
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77375-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77375-001-03 118 mL in 1 TUBE; Type 0: Not a Combination Product 05/06/2020 2 NDC:77375-001-01 30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/06/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/06/2020 Labeler - Evora Worldwide (081336028) Establishment Name Address ID/FEI Business Operations Inspec Solutions LLC 081030372 manufacture(77375-001)