Label: EO HAND SANITIZER SWEET ORANGE- alcohol spray
- NDC Code(s): 54748-103-02, 54748-103-05, 54748-103-09
- 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 19, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients:
- Purpose:
- Uses:
- Warnings:
- KEEP OUT OF REACH OF CHILDREN
- Directions:
- Other Information:
- Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
ESSENTIAL OILS
USDA ORGANIC
HAND sanitizer SPRAY
sweet orange
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
EO® PRODUCTS
SMALL WORLD TRADING CO. SAN RAFAEL, CA 94901
MADE IN THE USA FROM DOMESTIC AND GLOBALLY SOURCED INGREDIENTS
800-570-3775 eoproducts.com
CERTIFIED ORGANIC BY CCOF
- Packaging
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INGREDIENTS AND APPEARANCE
EO HAND SANITIZER SWEET ORANGE
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54748-103 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) ORANGE OIL (UNII: AKN3KSD11B) LEMON OIL (UNII: I9GRO824LL) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54748-103-02 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/15/2013 11/30/2016 2 NDC:54748-103-05 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/02/2017 3 NDC:54748-103-09 6 in 1 BOX 08/13/2018 3 NDC:54748-103-05 59 mL in 1 BOTTLE, SPRAY; 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 01/15/2013 Labeler - EO Products, LLC (786611210) Establishment Name Address ID/FEI Business Operations EO Products, LLC 786611210 manufacture(54748-103)