Label: EO HAND SANITIZER LAVENDER- alcohol spray
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NDC Code(s):
54748-101-01,
54748-101-02,
54748-101-05,
54748-101-08, view more54748-101-09, 54748-101-12
- Packager: EO Products, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 29, 2023
If you are a consumer or patient please visit this version.
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- Drug Facts
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- Directions:
- Other Information:
- Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
ESSENTIAL OILS
ORGANIC SPRAY
french lavender
99.9% EFFECTIVE AGAINST MOST COMMON GERMS
made with moisturizing ingredients
SYNTHETIC FRAGRANCE FREE
TRICLOSAN FREE • BENZALKONIUM CHLORIDE FREE
MADE WITH ORGANIC INGREDIENTS • PHTHALATE FREE
Inviting Self-care
the scent benefit
French lavender draws you into the present moment, the now–an inspired daily dose of serenity.the body benefit
99.9% effective against most common germs. Non-drying vegetable glycerin smoothes skin without leaving a heavy residue behind.Certified corporation™
Cruelty Free
CERTIFIED GLUTEN FREE
100% RECYCLED BOTTLE
We’ve consciously crafted accessible, timeless self-care rituals since 1995– all made with love, and without parabens, phthalates or synthetic fragrances.
EO®PRODUCTS, LLC. SAN RAFAEL, CA 94901
MADE IN THE USA FROM DOMESTIC AND GLOBALLY SOURCED COMPONENTS
800-570-3775 eoproducts.com
CERTIFIED ORGANIC BY CCOF
- Packaging
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INGREDIENTS AND APPEARANCE
EO HAND SANITIZER LAVENDER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-101 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) LAVENDER OIL (UNII: ZBP1YXW0H8) ECHINACEA ANGUSTIFOLIA LEAF (UNII: FS7G8S6PJ8) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-101-01 10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/15/2013 2 NDC:54748-101-12 12 in 1 BOX 08/13/2018 2 NDC:54748-101-01 10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 3 NDC:54748-101-02 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/15/2013 10/31/2016 4 NDC:54748-101-05 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/02/2017 5 NDC:54748-101-09 6 in 1 BOX 08/13/2018 5 NDC:54748-101-05 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 6 NDC:54748-101-08 237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/15/2013 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-101)