Label: EVERYONE HAND SANITIZER PEPPERMINT CITRUS- alcohol gel
- NDC Code(s): 54748-402-02, 54748-402-05, 54748-402-09
- Packager: EO Products, LLC
- Category: HUMAN OTC DRUG LABEL
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 February 22, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
- Directions:
-
Inactive Ingredients:
Purified Water, Vegetable Glycerin, EO® Essential Oil Blend [Citrus Aurantium Dulcis (Orange) Peel Oil, Lavandula Angustifolia (Lavender) Oil, Mentha Piperita (Peppermint) Oil], Organic Simmondsia Chinensis (Jojoba) Seed Oil, Carbomer, Dimethicone, Aminomethyl Propanol, *Limonene
*component of essential oil
- Other Information:
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
EVERYONE HAND SANITIZER PEPPERMINT CITRUS
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-402 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ORANGE OIL (UNII: AKN3KSD11B) LAVENDER OIL (UNII: ZBP1YXW0H8) PEPPERMINT OIL (UNII: AV092KU4JH) JOJOBA OIL (UNII: 724GKU717M) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) DIMETHICONE (UNII: 92RU3N3Y1O) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) LIMONENE, (+)- (UNII: GFD7C86Q1W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-402-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/07/2013 02/15/2017 2 NDC:54748-402-05 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/31/2018 3 NDC:54748-402-09 6 in 1 PACKAGE 08/31/2018 3 NDC:54748-402-05 59 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/07/2013 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-402)