Label: EVERYONE HAND SANITIZER WIPES LAVENDER ALOE- alcohol cloth
- NDC Code(s): 54748-505-15
- Packager: EO Products, 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 February 22, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients:
- Purpose:
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
everyone® for everyboby
99.9% EFFECTIVE against most common germs
PLANT BASED PURE ESSENTIAL OILS
lavender+aloe
NOPE!
- no synthetic fragrance
- no triclosan
- no phthalates
- no animal testing
YEP!
- biodegradable*
- plant extracts
- pure essential oils
- sugar cane-derived alcohol
everyone® is welcome.
Follow us: everyoneproducts
eoproducts.com
everyone® loves clean hands
*90% biodegradable within 60 days in municipal/industrial facilities according to OECD 311 standards.
Certified Gluten-Free® Cruelty Free™ Certified Corporation™
EO® PRODUCTS
Small World Trading Co.San Rafael, CA 94901
Made in the USA From Domestic and Globally Sourced Components
800-570-3775 eoproducts.com
- Packaging
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INGREDIENTS AND APPEARANCE
EVERYONE HAND SANITIZER WIPES LAVENDER ALOE
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-505 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.62 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAVENDER OIL (UNII: ZBP1YXW0H8) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) WHITE TEA (UNII: O0M3396E09) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-505-15 6 in 1 BOX 08/01/2020 1 15 in 1 POUCH 1 3 mL in 1 PACKAGE; 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 08/01/2020 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-505)