Label: EVERYONE HAND SANITIZER- alcohol spray
- NDC Code(s): 54748-305-04, 54748-305-07
- Packager: EO Products, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 11, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- Directions:
- Other Information:
- Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
for everybody
99.9%
EFFECTIVE
against most common germsunscented
Better for you means better for everyone. That’s why Everyone doesn’t believe in using fake ingredients that are impossible to pronounce. This sanitizer relies on gentle but effective ingredients that are free from added fragrances or aromatic irritants. It’s even better when shared.
NOPE!
• no synthetic fragrance
• no triclosan
• no phthalates
• no animal testingYEP!
• unscented
• moisturizing
• sugar cane derived alcohol
• zero-waste manufacturingDIRECTIONS: Every spray keeps a worry at bay. Have our 32oz hand sanitizer spray handy for any palm in need (yours included). Just spray and massage into the skin for gentle protection you can feel.
EO® PRODUCTS
Small World Trading Co.
San Rafael, CA 94901
Made in the USA From Domestic and Globally Sourced Components
800-570-3775Follow us: everyoneproducts
eoproducts.com
Certified Corporation
Certified Gluten-Free
CRUELTY FREE
EWG VERIFIED
FOR YOUR HEALTH
EWG.ORG - Packaging
-
INGREDIENTS AND APPEARANCE
EVERYONE HAND SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-305 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-305-07 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/01/2020 2 NDC:54748-305-04 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/01/2020 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-305)