Label: EVERYONE HAND SANITIZER COCONUT LEMON- ethyl alcohol spray
- NDC Code(s): 54748-601-05, 54748-601-07, 54748-601-08, 54748-601-09
- Packager: EO Products, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 20, 2025
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- Drug Facts
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- Directions:
- Other Information:
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Inactive Ingredients:
*Aloe Barbadensis Leaf Juice, *Calendula Officinalis Flower Extract, *Camellia Sinensis (White Tea) Leaf Extract, Citrus Medica Limonum (Lemon) Peel Oil, ‡Gamma Nonalactone, ‡Gamma Octalactone, Glycerin, ‡Heliotropine, †Limonene, *Matricaria Recutita (Chamomile) Flower Extract, ‡Vanillin, Water
*organic †component of essential oil ‡component of organic coconut flavor extract
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SPL UNCLASSIFIED SECTION
Cruelty Free
VEGAN
everyone is welcome®
Follow us: everyoneproducts
loveeveryone.com
EO® PRODUCTS, LLC
San Rafael, CA 94901Made in the USA from domestic and globally sourced components.
800-570-3775
everyone loves clean hands
WE LOVE ESSENTIAL OILS SINCE 1995
99.9% EFFECTIVE against most common germs
✓ gluten-free
✓ sugar cane-derived alcohol
✓ made with love
- Packaging
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INGREDIENTS AND APPEARANCE
EVERYONE HAND SANITIZER COCONUT LEMON
ethyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-601 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 ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) WHITE TEA (UNII: O0M3396E09) LEMON OIL, COLD PRESSED (UNII: I9GRO824LL) .GAMMA.-NONALACTONE (UNII: I1XGH66S8P) .GAMMA.-OCTALACTONE (UNII: UHD6M52X0K) GLYCERIN (UNII: PDC6A3C0OX) PIPERONAL (UNII: KE109YAK00) LIMONENE, (+)- (UNII: GFD7C86Q1W) CHAMOMILE (UNII: FGL3685T2X) VANILLIN (UNII: CHI530446X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-601-09 6 in 1 BOX 01/25/2021 1 NDC:54748-601-05 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 2 NDC:54748-601-08 237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/25/2021 3 NDC:54748-601-07 946 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/25/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/25/2021 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-601)


