Label: ELYPTOL HAND SANITIZER WIPE- ethanol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 69343-322-01, 69343-322-06, 69343-322-10, 69343-322-24, view more69343-322-60 - Packager: Elyptol Inc.
- 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 December 22, 2021
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- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Inactive Ingredients
- Purpose
- Warnings
- Directions
- KEEP OUT OF REACH OF CHILDREN
- Other Information
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- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
ELYPTOL HAND SANITIZER WIPE
ethanol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69343-322 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69343-322-24 24 in 1 CARTON 12/15/2016 1 NDC:69343-322-01 1 in 1 POUCH; Type 0: Not a Combination Product 2 NDC:69343-322-06 6 in 1 CARTON 12/15/2016 2 NDC:69343-322-10 10 in 1 PACKET; Type 0: Not a Combination Product 3 NDC:69343-322-60 6 in 1 CARTON 08/01/2017 3 1 in 1 CANISTER; 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 12/15/2016 Labeler - Elyptol Inc. (079594781)