Label: HAND SANITIZER WIPES- alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 75214-501-20, 75214-501-50, 75214-501-80 - Packager: HANUL CO.,LTD
- 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 January 9, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER WIPES
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75214-501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 1.83 mL in 100 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.002 mL in 100 mL WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75214-501-50 334 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/30/2020 2 NDC:75214-501-20 134 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/30/2020 3 NDC:75214-501-80 534 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/30/2020 Labeler - HANUL CO.,LTD (557814370) Establishment Name Address ID/FEI Business Operations HANUL CO.,LTD 557814370 manufacture(75214-501)
